| Molecular detection of a Yp/18 translocation in a 45,X holoprosencephalic male |
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| Chromosome localization of the human insulin gene in transgenic mouse lines |
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| NsiI andScaI restriction fragment length polymorphisms at the atrial natriuretic peptides (ANP) gene locus |
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| MspI andHindIII restriction fragment length polymorphisms at the human Na,K-ATPase β-subunit (ATP1B) gene locus |
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| Erratum |
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| Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries |
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| Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes |
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| Segregation of lymphocyte low-molecular-weight DNA and antinuclear-antibodies in a family with systemic lupus erythematosus in first cousins |
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| DNA polymorphism haplotypes of the human apolipoprotein APOA1-APOC3-APOA4 gene cluster |
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| Regional mapping to 4q32.1 by in situ hybridization of a DNA domain rearranged in human liver cancer |
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| Trisomy 21q223 and Down's phenotype correlation evidenced by in situ hybridization |
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| Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11 |
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| Apolipoprotein E polymorphism in the Netherlands and its effect on plasma lipid and apolipoprotein levels |
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| The gene encoding the large human neurofilament subunit (NF-H) maps to the q121–q131 region on human chromosome 22 |
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| X-Y crossing over in the chimpanzee |
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| Detection of a rare-cutter RFLP in a CpG-rich island near the cystic fibrosis locus |
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| Genetic mapping of four DNA markers (DXS16, DXS43, DXS85, and DXS143) from the p22 region of the human X chromosome |
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| Gene dosage evidence for the regional assignment of GPT (glutamate-pyruvate transaminase; E. C. 2.6.1.2) locus to 8q24.2→8qter |
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| The presence of a reduced amount of 32-kd “protective” protein is a distinct biochemical finding in late infantile galactosialidosis |
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| Announcement |
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| Characteristics of Mongoloid and neighboring populations based on the genetic markers of human immunoglobulins |
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| The microtubular cytoskeleton and chromosomes of unfertilized human oocytes aged in vitro |
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| Non-random chromosomal aberrations in a complex leukaemic clone of a Bloom's syndrome patient |
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| SCE variability in lymphocytes and fibroblasts |
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| Cell cycle studies in chorionic villi |
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| Spontaneous and induced chromosomal instability in Werner syndrome |
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| Prevalence and molecular heterogeneity of alfa+thalassemia in two tribal populations from Andhra Pradesh, India |
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| Familial translocation t(17;22), including the segregation in five consecutive abortuses |
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| Zellweger syndrome and a microdeletion of the proximal long arm of chromosome 7 |
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| Deletion 11q23.3 without familial predisposition |
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| Genetic determination of the human EEG |
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| Linkage analysis in X-linked ichthyosis (steroid sulfatase deficiency) |
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| An unusual variant of chromosome 16 |
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| A new rare distamycin a-inducible fragile site, fra(11)(p15.1), found in two acute nonlymphocytic leukemia (ANLL) patients with t(7;11)(p15-p13;p15) |
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| Retinal/macular pigmentation in conjunction with ring 14 chromosome |
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| A frequent factor XII gene mutation in Hageman trait |
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| Patterns of exon deletions in Duchenne and Becker muscular dystrophy |
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| Orosomucoid (alpha-1 acid glycoprotein) phenotyping by use of immobilized pH gradients with 8M urea and immunoblotting |
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| Mapping of the human retinoic acid receptor to the q21 band of chromosome 17 |
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| Assignment of the humanhap retinoic acid receptor RARβ gene to the p24 band of chromosome 3 |
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| A new RFLP withStuI and probe cX55.7 (DXS105) and its usefulness in carrier analysis of fragile X syndrome |
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| Siblings with chromosome mosaicism, microcephaly, and growth retardation: the phenotypic expression of a human mitotic mutant? |
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| Pericentric inversion of chromosome 19 in three families |
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| Announcements |
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| Sorting of chromosomes by magnetic separation |
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| Restriction endonuclease mapping of six novel deletions of the factor VIII gene in hemophilia A |
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| Localization of DNA probes with tight linkage to the cystic fibrosis locus by in situ hybridization using fibroblasts with a 7q22 deletion |
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| Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal marker |
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| No predictive value of GC phenotypes for HIV infection and progression to AIDS |
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| X-chromosome polysomy in the male |
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| Hemoglobin F production in heterocellular hereditary persistence of fetal hemoglobin and its linkage to the ? globin gene complex |
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| ?-Globin gene linked DNA haplotypes and frameworks in three South-East Asian populations |
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| Chondrodysplasia punctata with X;Y translocation |
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| A substitution of cytosine for thymine in codon 110 of the human ?-globin gene is a novel cause of ?-thalassemia phenotypes |
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| Myopia and intelligence:a pleiotropic relationship? |
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| Mapping of the Emery-Dreifuss gene through reconstruction of crossover points in two Italian pedigrees |
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| Allelic association of the cystic fibrosis locus and two DNA markers, XV2c and KM19, in 55 German families |
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| Fluorescence in situ hybridization and Y ring chromosome |
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| Recurrent genomic rearrangements are not at the fragile sites on chromosomes 3 and 5 in human renal cell carcinomas |
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| BglII RFLPs in the COL1A2 gene in the Finnish population |
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| HLA class I and H ferritin gene polymorphisms in normal subjects and patients with haemochromatosis |
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| The parental origin and mechanism of formation of three dicentric X chromosomes |
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| Xp21 DNA microdeletion in a patient with chronic granulomatous disease, retinitis pigmentosa, and McLeod phenotype |
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| Heterozygosity and localisation of normal allelic fragments for an alpha1-antitrypsin homologous sequence |
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| TaqI polymorphism in the LDL receptor gene and a TaqI 1.5-kb band associated with familial hypercholesterolemia |
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| Nephrogenic diabetes insipidus: close linkage with markers from the distal long arm of the human X chromosome |
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| Kenny syndrome: description of additional abnormalities and molecular studies |
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| Deletion of chromosome region 13q14 is transmissible and does not always predispose to retinoblastoma |
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| Use of linkage disequilibrium data in prenatal diagnosis of cystic fibrosis |
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| Further evidence for localization of the gene of erythrokeratodermia variabilis |
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| PI Scologne: a new variant in the alpha-1-antitrypsin system |
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| Miller-Dieker syndrome and monosomy 17p13:a new case |
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| Maple syrup urine disease: a possible biochemical basis for the clinical heterogeneity |
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| XX sex reversal in the American cocker spaniel dog: phenotypic expression and inheritance |
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|
| Maternal levels of pregnancy-specific ?1 (SP-1) are elevated in pregnancies affected by Down's syndrome |
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|
| Tight linkage between myotonic dystrophy and apolipoprotein E genes revealed with allele-specific oligonucleotides |
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| Cytogenetic analysis of sperm from a male heterozygous for a 13;14 Robertsonian translocation |
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| Lysinuric protein intolerance mutation is not expressed in the plasma membrane of erythrocytes |
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| Assignment of human platelet GP2B (GPIIb) gene to chromosome 17, region q21.1-q21.3 |
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|
| Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes |
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| Different numbers of maternal and paternal siblings of cystic fibrosis patients |
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| Interstitial deletion of chromosome 15: two cases |
|
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| The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK |
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|
|
| A new LDL receptor gene deletion mutation in the South African population |
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|
|
| Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardation |
|
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|
| Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q |
|
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|
|
| Synergistic effect of hydroxyurea and excessive thymidine on the expression of the common fragile sites at 3p14 and 16q23 |
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|
|
| Glucose-6-phosphate dehydrogenase variants and their frequency in Guangdong, China |
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|
|
| Pelizaeus-Merzbacher disease: identification of heterozygotes with magnetic resonance imaging? |
|
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|
|
| Galactosialidosis: molecular heterogeneity in biosynthesis and processing of protective protein for ?-galactosidase |
|
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|
|
| Familial amyloidotic polyneuropathy: transthyretin (prealbumin) variants in kindreds of Italian origin |
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|
|
Italian origin |
| Population cytogenetics of folate-sensitive fragile sites |
|
|
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|
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|
|
| The pathology of trisomy 13 syndrome |
|
|
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|
|
| Human mitochondrial DNA types in Finland |
|
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|
|
| Blastomere karyotyping and transfer of chromosomally selected embryos |
|
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|
|
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|
|
| Use of restriction fragment length polymorphic probes in the analysis of Down's syndrome trisomy |
|
|
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|
|
|
|
|
|
| Assignment of human coagulation factor XII (fXII) to chromosome 5 by cDNA hybridization to DNA from somatic cell hybrids |
|
|
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|
|
|
|
|
| Type I procollagen in the severe non-lethal form of osteogenesis imperfecta |
|
|
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|
|
|
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|
|
| A complete deletion of the factor IX gene and new TaqI variant in a hemophilia B kindred |
|
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|
|
|
|
|
| Three major cytogenetic subgroups can be identified among chromosomally abnormal solitary lipomas |
|
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|
|
| Polymorphism of MHC class III genes: definition of restriction fragment linkage groups and evidence for frequent deletions and duplications |
|
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|
|
|
|
|
|
| Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndrome |
|
|
|
|
|
|
|
|
|
| Analysis for linkage between F13A and three chromosome 6 marker loci: evidence for 6pter: F13A:HLA:GL01:cen gene order |
|
|
|
|
|
|
|
|
|
| Spermatogenesis in two patients with the fragile X syndrome |
|
|
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|
|
|
|
|
|
| A recombinant X chromosome in a short statured girl resulting from a maternal pericentric inversion |
|
|
|
|
|
|
|
|
|
| Restriction fragment length polymorphisms detected by anonymous DNA probes mapped to defined intervals of human chromosome 16 |
|
|
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|
|
|
|
|
| The human tyrosine aminotransferase gene: characterization of restriction fragment length polymorphisms and haplotype analysis in a family with tyrosinemia type II |
|
|
|
|
|
|
|
|
|
| Molecular analysis of a reciprocal translocation t(5;11)(q11;p13) in a WAGR patient |
|
|
|
|
|
|
|
|
|
| Increased amounts of small polydisperse circular DNA (spcDNA) in angiofibroma-derived cell cultures from patients with tuberous sclerosis (TS) |
|
|
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|
|
|
|
|
|
| Publication of DNA variants |
|
|
|
|
|
|
|
|
|
| Isolation of DNA sequences on human chromosome 21 by application of a recombination-based assay to DNA from flow-sorted chromosomes |
|
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|
|
|
|
|
|
| cDNA cloning, expression and mapping of human laminin B2 gene to chromosome 1q31 |
|
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|
|
|
|
|
|
|
| Effect of caffeine in Fanconi anemia |
|
|
|
|
|
|
|
|
|
| Comparison between the allelic frequency distribution of the Ha-ras 1 locus in normal individuals and patients with lymphoma, breast, and ovarian cancer |
|
|
|
|
|
|
|
|
|
| Human satellite-III DNA: an example of a ?macrosatellite? polymorphism |
|
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|
|
|
|
|
|
| Regional chromosomal localisation of APOA2 to 1q21–1q23 |
|
|
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|
|
|
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|
|
| Linkage between the variegate porphyria (VP) and the alpha-1-antitrypsin (PI) genes on human chromosome 14 |
|
|
|
|
|
|
|
|
|
| Publication of DNA variants |
|
|
|
|
|
|
|
|
|
| Small metacentric marker chromosomes, particularly isochromosomes, in cancer |
|
|
|
|
|
|
|
|
|
| High efficiency in the attribution of parental origin of non-disjunction in trisomy 21 by both cytogenetic and molecular polymorphisms |
|
|
|
|
|
|
|
|
|
| Restriction fragment length polymorphisms associated with factor VIII: C gene in Chinese |
|
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|
|
✓ |
|
Chinese |
| The ras-related ral gene maps to chromosome 7p15-22 |
|
|
|
|
|
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|
|
|
| Human esterase D gene: complete cDNA sequence, genomic structure, and application in the genetic diagnosis of human retinoblastoma |
|
|
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|
|
|
|
|
|
| Individual specific DNA fingerprints from a hypervariable region probe: alpha-globin 3?HVR |
|
|
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|
|
|
|
|
|
| Acquired chromosome rearrangements in human lymphocytes: effect of aging |
|
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|
|
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|
|
| Chromosome abnormalities in tuberous sclerosis |
|
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|
|
| Arabinofuranosyl nucleosides induce common fragile sites |
|
|
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|
|
|
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|
|
| Agyria ? pachygyria and Miller-Dieker syndrome: clinical, genetic and chromosome studies |
|
|
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|
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|
|
| Chromosome localization and polymorphism of an oestrogen-inducible gene specifically expressed in some breast cancers |
|
|
|
|
|
|
|
|
|
| Haemoglobin freiburg: direct detection by synthetic oligonucleotide probes |
|
|
|
|
|
|
|
|
|
| Chromosomal localization of the gene for human glucosamine-6-sulphatase to 12q14 |
|
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|
|
|
|
|
|
| Can sister chromatid intercrossings be considered as prelesions? |
|
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|
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|
|
| Human factor H (?1H-globulin): linkage analysis |
|
|
|
|
|
|
|
|
|
| Close linkage of a highly polymorphic marker (D5S37) to familial adenomatous polyposis (FAP) and confirmation of FAP localization on chromosome 5q21-q22 |
|
|
|
|
|
|
|
|
|
| Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome |
|
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|
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|
|
|
|
| Prenatal diagnosis of alpha-1-antitrypsin deficiency using oligonucleotide probe analysis |
|
|
|
|
|
|
|
|
|
| Chromosomal rearrangement involving chromosomes 4, 6, 11 and 11 |
|
|
|
|
|
|
|
|
|
| C-anaphases in lymphocyte cultures versus premature centromere division syndromes |
|
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|
|
|
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|
|
| Population cytogenetics of rare fragile sites in Japan |
|
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|
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|
|
| Mutations of the low density lipoprotein receptor in Japanese kindreds with familial hypercholesterolemia |
|
|
|
|
|
|
|
|
|
| Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease |
|
|
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|
|
|
|
|
|
| Types, rates, origin and expressivity of chromosome mutations involving 13q14 in retinoblastoma patients |
|
|
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|
|
|
|
|
|
| Shwachman syndrome and chromosome breakage |
|
|
|
|
|
|
|
|
|
| Assignment of the human fast skeletal muscle myosin alkali light chains gene (MLC1F/MLC3F) to 2q 32.1-2qter |
|
|
|
|
|
|
|
|
|
| Genomic structure and evolution of the human pepsinogen A multigene family |
|
|
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|
|
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|
|
| Transposition of c-abl oncogene in a case of masked Ph chromosome duplicated in blastic phase |
|
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|
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|
|
| Fluorescence in situ hybridization to interphase cell nuclei in suspension allows flow cytometric analysis of chromosome content and microscopic analysis of nuclear organization |
|
|
|
|
|
|
|
|
|
| c-Ha-ras-1 alleles in bladder cancer, Wilms' tumour and malignant melanoma |
|
|
|
|
|
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|
|
| A regional localisation for an X-linked suppressor gene (XS) for the Lutheran blood group |
|
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|
|
|
|
|
| Localization of the villin gene on human chromosome 2q35-q36 and on mouse chromosome 1 |
|
|
|
|
|
|
|
|
|
| Localization of the human G-CSF gene to the region of a breakpoint in the translocation typical of acute promyelocytic leukemia |
|
|
|
|
|
|
|
|
|
| Recurrent t(11;22) breakpoint mapping by chromosome flow sorting and spot-blot hybridization |
|
|
|
|
|
|
|
|
|
| Further localization of ETS1 indicates that the chromosomal rearrangement in Ewing sarcoma does not occur at fra(11)(q23) |
|
|
|
|
|
|
|
|
|
| Loss of der(3) in renal carcinoma cells of a patient with constitutional t(3;12) |
|
|
|
|
|
|
|
|
|
| The CpG dinucleotide and human genetic disease |
|
|
|
|
|
|
|
|
|
| Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia |
|
|
|
|
|
|
|
|
|
| Localization of the active gene of aldolase on chromosome 16, and two aldolase A pseudogenes on chromosomes 3 and 10 |
|
|
|
|
|
|
|
|
|
| A BrdU-requiring fragile site on chromosome 12 |
|
|
|
|
|
|
|
|
|
| The position of the gene locus for monocyte alloantigens (HMA system) on chromosome 6 |
|
|
|
|
|
|
|
|
|
| The peculiar spectrum of ?-thalassemia genes in Tunisia |
|
|
|
|
|
|
|
|
|
| Analysis of crossover type in the ?-3�7 haplotype among sickle cell anemia patients from various parts of Africa |
|
|
|
|
|
|
|
|
|
| Frequency of tri- and multiradial configurations in fragile X chromosomes |
|
|
|
|
|
|
|
|
|
| Aphidicolin, DNA repair, and fragile sites |
|
|
|
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|
|
|
|
|
| Aberrant breakpoints in chronic myelogenous leukemia; oncogenes and fragile sites |
|
|
|
|
|
|
|
|
|
| A disease with features of cutis laxa and Ehlers-Danlos syndrome |
|
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| ?-thalassemia mutations in the Portuguese population |
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✓ |
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Portuguese population |
| Genetic transferrin types and iron-binding: a comparative study of a European and an African population sample |
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✓ |
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a European and an African population sample |
| Fragile sites induced by FUdR, caffeine, and aphidicolin |
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| Organization and genomic distribution of ?82H? alpha satellite DNA |
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| Molecular characterization of different ataxia telangiectasia T-cell clones |
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| Genetics of the quantitative Lp(a) lipoprotein trait |
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| Fanconi's anaemia: correlation of genetic complementation group with psoralen/UVA response |
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| Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, OTC, 754, XJ-1.1, pERT87, and C7 |
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| Chromosomal radiosensitivity of Down syndrome lymphocytes at different stages of the cell cycle |
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| Assignment of the human progesterone receptor to the q22 band of chromosome 11 |
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| G6PD Viangchan: a new glucose 6-phosphate dehydrogenase variant from Laos |
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| Absence of charge variants in human skeletal muscle enzymes of the glycolytic pathway |
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| Trichothiodystrophy, xeroderma pigmentosum and PIBI(D)S syndrome |
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| Editorial help |
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| Multilocus analysis of the fragile X syndrome |
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| Turner's syndrome: a qualitative and quantitative analysis of EEG background activity |
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| DNA linkage analysis of X-linked retinoschisis |
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| Homozygous osteogenesis imperfecta unlinked to collagen I genes |
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| Heat resistance, immunological and quantitative changes of neutrophil alkaline phosphatase in trisomy 21 pregnancies |
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| A physical map of the apolipoprotein gene cluster on human chromosome 19 |
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| Association of a new chromosomal deletion [del(1)(q32q42)] with diaphragmatic hernia: assignment of a human ferritin gene |
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| Linkage of a polymorphic marker for the type III collagen gene (COL3A1) to atypical autosomal dominant Ehlers-Danlos syndrome type IV in a large Belgian pedigree |
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| Germinal mosaicism in Duchenne muscular dystrophy |
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| Parental centromere separation sequence and aneuploidy in the offspring |
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| Evidence for linkage equilibrium between two RFLPs associated with the human SST locus |
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| Recombination frequencies between Duchenne muscular dystrophy and intragenic markers in multigeneration families |
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| Announcement |
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| The molecular basis of HbH disease in Taiwan |
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| Common genetic pools between human populations |
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| The use of DNA probes to establish parental origin in Down syndrome |
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| Investigation of three XX males by cytogenetic and DNA analyses |
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| Linkage of the DNA-segment D7S13 (pB79a) with the cystic fibrosis locus |
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| Facts and considerations about sex-specific antigens |
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| Heterozygosity and ethnic variation in Japanese platelet proteins |
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| Molecular basis of ? thalassemia in South China |
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| Genetics of the quantitative Lp(a) lipoprotein trait |
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| A DNA polymorphism of an apoprotein gene associates with the hypertriglyceridaemia of primary gout |
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| The Duffy blood group is linked to the α-spectrin locus in a large pedigree with autosomal dominant inheritance of Charcot-Marie-Tooth disease type 1 |
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| Feto-maternal transfusion after chorionic villus sampling |
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| Alterations of class I HLA genes in human colon cancers |
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| Apolipoprotein gene cluster on chromosome 19 |
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| Localization of the spherocytosis gene to chromosome segment 8p11.22?8p21.1 |
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| Prevalence of the 281 (Gly→Glu) mutation in hepatoerythropoietic porphyria and porphyria cutanea tarda |
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| Multiple recurrence of trisomy 21 Down syndrome |
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| BglII RFLPs in the COL1A2 gene in the Finnish population |
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✓ |
|
Finnish population |
| Linkage disequilibrium analyses and restriction mapping of four RFLPs at the pro?2(I) collagen locus: lack of correlation between linkage disequilibrium and physical distance |
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| Deletion proximal to DXS68 locus (L1 probe site) in a boy with Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal hypoplasia |
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| A PvuII polymorphism in the 5? flanking region of the apolipoprotein AIV gene: its use to study genetic variation determining serum lipid and apolipoprotein concentration |
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| The possible role of meiotic pairing anomalies in the atresia of human fetal oocytes |
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| Prenatal diagnosis of cystic fibrosis by microvillar enzyme assay on a sequence of 258 pregnancies |
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| Nebulin seen in DMD males including one patient with a large DNA deletion encompassing the DMD gene |
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| A ?new? allele of esterase D in a retinoblastoma family |
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| Concurrence of the triple-X syndrome and expression of the fragile site Xq27.3 |
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| A report of four different unusual 6-PGD electrotypes in Caucasian and Negro populations |
✓ |
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|
✓ |
|
Negro populations |
| Molecular characterization of a Y;15 translocation segregating in a family |
|
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| DA/DAPI-Fluorescent heteromorphism of human Y chromosome |
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| Replication kinetics of X chromosomes in fibroblasts and lymphocytes |
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| X Chromosome deletions detectable by flow cytometry in some patients with steroid sulphatase deficiency (X-linked ichthyosis) |
|
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| Cystic fibrosis: screening for a DNA deletion by field inversion gel electrophoresis |
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| Detection of a new hybrid ?2 globin gene among American Blacks |
|
|
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|
✓ |
|
American Blacks |
| C-anaphases rediscovered |
|
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| Sperm chromosome complements in a 47,XYY man |
|
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| Relationships between DNA and protein polymorphisms of apolipoprotein B |
|
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| Evolutionary conservation of the human homologue of the yeast cell cycle control gene cdc2 and assignment of Cd2 to chromosome 10 |
|
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|
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| Assignment of the complement serine protease genes C1r and C1s to chromosome 12 region 12p13 |
|
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|
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| A new glucose-6-phosphate dehydrogenase variant (G6PD Tsukui) associated with congenital hemolytic anemia |
|
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| Localization of the human c-kit protooncogene on the q11?q12 region of chromosome 4 |
|
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|
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| Publication of DNA variants |
|
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| Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11 |
|
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|
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| Neuropsychological deficits in obligatory heterozygotes for metachromatic leukodystrophy |
|
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| A frequent A?-persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with ?-thalassemia |
|
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|
|
| Human sperm chromosome studies in a reciprocal translocation t(2;5) |
|
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| Identification of a single nucleotide change in a mutant gene for hypoxanthine-guanine phosphoribosyltransferase (HPRTAnn Arbor) |
|
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|
|
| Mitochondrial DNA polymorphism in mitochondrial myopathy |
|
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| Family resemblance for serum uric acid in a Jerusalem sample of families |
|
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|
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| Mutations for the autosomal recessive and autosomal dominant forms of polycystic kidney disease are not allelic |
|
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|
|
| Cystic fibrosis typing with DNA probes: experience of a screening laboratory |
|
|
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|
|
| Linkage between the loci for the Lp(a) lipoprotein (LP) and plasminogen (PLG) |
|
|
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|
|
|
|
| Variation in spontaneous chromosomal damage as a function of biologic rhythms in women |
|
|
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|
|
| Characterization of a partial deletion of the factor VIII gene in a haemophiliac with inhibitor |
|
|
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|
|
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|
|
| The tyrosinase-positive oculocutaneous albinism locus is not linked to the ?-globin locus in man |
|
|
|
|
|
|
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|
|
| G6PD Huntsville: a new glucose-6-phosphate dehydrogenase associated with chronic hemolytic anemia |
|
|
|
|
|
|
|
|
|
| Deletion 2q31.3?2q33.3: gene dosage effect of ribulose 5-phosphate 3-epimerase |
|
|
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|
|
|
|
|
|
| Reply to the letter by Y. Chamla, C-anaphases rediscovered |
|
|
|
|
|
|
|
|
|
| DNA polymorphism and the study of disease associations |
|
|
|
|
|
|
|
|
|
| Molecular characterization of ataxia telangiectasia T cell clones |
|
|
|
|
|
|
|
|
|
| Chromosome abnormalities in peripheral blood lymphocytes from untreated Hodgkin's patients |
|
|
|
|
|
|
|
|
|
| Linkage heterogeneity and fragile X |
|
|
|
|
|
|
|
|
|
| Linkage disequilibrium between mutation and RFLP haplotype at the phenylalanine hydroxylase locus in the German population |
|
|
|
|
|
|
|
|
|
| X-linked cleft palate: the gene is localized between polymorphic DNA markers DXYS12 and DXS17 |
|
|
|
|
|
|
|
|
|
| A HindIII RFLP and a gene lesion in the coagulation factor VIII gene |
|
|
|
|
|
|
|
|
|
| DNA polymorphism unique for a complotype with deletion of HLA-linked C4B and 21-hydroxylase B genes causing congenital adrenal hyperplasia |
|
|
|
|
|
|
|
|
|
| Characterization of a (Y;4) translocation by DNA hybridization |
|
|
|
|
|
|
|
|
|
| PGM2 *2 (Atkinson) exists in Germany |
|
|
|
|
|
|
|
|
|
| Chromosome breakage in control and fragile X subjects using folate-deficient culture conditions |
|
|
|
|
|
|
|
|
|
| Controversy concerning paternal age effect in 47,+21 Down's syndrome |
|
|
|
|
|
|
|
|
|
| Molecular evidence for true isochromosome 21q |
|
|
|
|
|
|
|
|
|
| Effects of folate in culture medium on common fragile sites in lymphocyte chromosomes from normal and leukemic children |
|
|
|
|
|
|
|
|
|
| Molecular evidence that the esterase-D gene lies proximal to the retinoblastoma susceptibility locus in chromosome region 13q14 |
|
|
|
|
|
|
|
|
|
| Inhibition of condensation in the late-replicating X chromosome induced by 5-azadeoxycytidine in human lymphocyte cultures |
|
|
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|
|
|
|
|
| The secretor locus as a marker for prenatal prediction of myotonic dystrophy (DM) |
|
|
|
|
|
|
|
|
|
| Linkage disequilibrium between RFLP haplotype 2 and the affected PAH allele in PKU families from the Berlin area of the German Democratic Republic |
|
|
|
|
|
|
|
|
|
| Phenylketonuria: distribution of DNA diagnostic patterns in German families |
|
|
|
|
|
|
|
|
|
| Announcement |
|
|
|
|
|
|
|
|
|
| Lesch-Nyhan syndrome: molecular investigation of three French Canadian families using a hypoxanthine-guanine phosphoribosyltransferase cDNA probe |
|
|
|
|
|
|
✓ |
|
French Canadian families |
| Isolation of human chromosome 21 sequences and their application to in situ hybridization |
|
|
|
|
|
|
|
|
|
| Spondyloepiphyseal dysplasia tarda: linkage with genetic markers from the distal short arm of the X chromosome |
|
|
|
|
|
|
|
|
|
| Family studies in scleroderma (systemic sclerosis) demonstrating an HLA-linked increased chromosomal breakage rate in cultured lymphocytes |
|
|
|
|
|
|
|
|
|
| Klinefelter's syndrome in Sardinia and Scotland |
|
|
|
|
|
|
|
|
|
| Assignment of ecto-5?-nucleotidase to human chromosome 6 |
|
|
|
|
|
|
|
|
|
| Genetic studies of low-abundance human plasma proteins |
|
|
|
|
|
|
|
|
|
| Editorial help |
|
|
|
|
|
|
|
|
|
| Molecular studies of haemophilia B in Sweden |
|
|
|
|
|
|
|
|
|
| Molecular characterization of ataxia telangiectasia T cell clones |
|
|
|
|
|
|
|
|
|
| A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphisms |
|
|
|
|
|
|
|
|
|
| Variability of human rRNA genes: inheritance and nonrandom chromosomal distribution of structural variants of nontranscribed spacer sequences |
|
|
|
|
|
|
|
|
|
| Increased methotrexate-induced chromosome breakage in patients with free trisomy 21 and their parents |
|
|
|
|
|
|
|
|
|
| Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours |
|
|
|
|
|
|
|
|
|
| Cystic fibrosis: typing 89 German families with linked DNA probes |
|
|
|
|
|
|
|
|
|
| DNA haplotypes of the human apoprotein B gene in coronary atherosclerosis |
|
|
|
|
|
|
|
|
|
| A mosaic 45,X/46,X,4(?) karyotype investigated with X and Y centromere-specific probes using a non-autoradiographic in situ hybridization technique |
|
|
|
|
|
|
|
|
|
| Linkage studies in X-linked Alport's syndrome |
|
|
|
|
|
|
|
|
|
| A new method for FXIIIA genetic variants determination using isoelectric focusing in 1 M urea |
|
|
|
|
|
|
|
|
|
| A family study of multiple mutations of alpha and delta glycophorins (glycophorins A and B) |
|
|
|
|
|
|
|
|
|
| Increased frequency of specific alleles of the c-Ha-ras gene in Japanese cancer patients |
|
|
|
|
|
|
|
|
|
| Immunoprecipitation of a male-specific polypeptide after in vitro translation of testicular poly(A)+ RNA |
|
|
|
|
|
|
|
|
|
| Bands involved in primary chromosome rearrangements in sarcomas are not constitutionally liable to breakage in sarcoma patients |
|
|
|
|
|
|
|
|
|
| Familial pericentric and paracentric inversions of chromosome 1 |
|
|
|
|
|
|
|
|
|
| XY sex reversal syndrome in the mare: clinical and behavioral studies, H-Y phenotype |
|
|
|
|
|
|
|
|
|
| The role of fluorinated pyrimidine analogues in the induction of the in vitro expression of the fragile X chromosome |
|
|
|
|
|
|
|
|
|
| A noninvasive method for determination of the sex and karyotype of the fetus from the maternal blood |
|
|
|
|
|
|
|
|
|
| Human apolipoprotein A-IV polymorphism: frequency and effect on lipid and lipoprotein levels |
|
|
|
|
|
|
|
|
|
| DNA haplotype distribution in Algerian ? thalassaemia patients |
|
|
|
|
|
|
|
|
|
| Origin of the extra chromosome in trisomy 18 |
|
|
|
|
|
|
|
|
|
| A dominantly inherited syndrome (microcephaly, short stature, peculiar facies, mental retardation) associated with two balanced rearrangements involving chromosomes 2;7 and 5;20 |
|
|
|
|
|
|
|
|
|
| Sperm chromosomal analysis after radiotherapy |
|
|
|
|
|
|
|
|
|
| Announcements |
|
|
|
|
|
|
|
|
|
| Publication of DNA variants |
|
|
|
|
|
|
|
|
|
| Expression of fragile sites in childhood acute lymphoblastic leukemia patients and normal controls |
|
|
|
|
|
|
|
|
|
| Maternal modulation of the inheritable meiosis I error Dipl I in mouse oocytes is associated with the type of mitochondrial DNA |
|
|
|
|
|
|
|
|
|
| The distribution of sex-specific (H-Y) antigens within the seminiferous tubules of the testis: an immunohistochemical study |
|
|
|
|
|
|
|
|
|
| The apolipoprotein(a) gene resides on human chromosome 6q26?27, in close proximity to the homologous gene for plasminogen |
|
|
|
|
|
|
|
|
|
| Breakage of the T cell receptor ? chain locus in non malignant clones from patients with ataxia telangiectasia |
|
|
|
|
|
|
|
|
|
| The coagulation factor VII regulator is located on 8p23.1 |
|
|
|
|
|
|
|
|
|
| DNA polymorphisms within the porphobilinogen deaminase gene in two Swedish families with acute intermittent porphyria |
|
|
|
|
|
|
|
|
|
| Linkage relationship between retinoschisis and four marker loci |
|
|
|
|
|
|
|
|
|
| Interstitial deletion of the short arm of chromosome 3 |
|
|
|
|
|
|
|
|
|
| Remarks to the letter from R. H. Martin |
|
|
|
|
|
|
|
|
|
| A cytogenetic study of mentally retarded school children in taiwan with special reference to the fragile X chromosome |
|
|
|
|
|
|
|
|
|
| Relationship between the number and function of human ribosomal genes |
|
|
|
|
|
|
|
|
|
| Interleukin 4 is at 5q31 and interleukin 6 is at 7p15 |
|
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|