| Localization of human c-mos to chromosome band 8q11 in leukemic cells with the t(8;21) (q22;q22) |
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| Detection of single-copy genes by nonisotopic in situ hybridization on human chromosomes |
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| Regional localization and molecular characterization of a DNA sequence on the long arm of chromosome 22 |
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| Genotyping of mitochondrial aldehyde dehydrogenase in blood samples using allele-specific oligonucleotides: comparison with phenotyping in hair roots |
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| Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM) |
|
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| Detection of 1q polysomy in interphase nuclei of human solid tumors with a biotinylated probe |
|
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| Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp |
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| Fragile sites and statistics |
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| Investigations of chorionic villi after chorionic villus sampling (CVS) |
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| Molecular deletion patterns in Duchenne and Becker type muscular dystrophy |
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| Rapid isolation of moderate and highly polymorphic DNA fragments mapping close to WT (Wilms' tumour) and AN2 (aniridia) on chromosome 11 |
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| Study of a family with a fragile site of the X chromosome at Xq27–28 without mental retardation |
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| Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screening |
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| Mutation analysis of β-thalassemia genes in a German family reveals a rare transversion in the first intron |
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| Induction of the fragile X on BrdU-substituted chromosomes with direct visualization of sister chromatid exchanges on banded chromosomes |
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| Confirmation and refinement of the localisation of the c-MEL locus on chromosome 19 by physical and genetic mapping |
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| Segregation frequency in microcephaly |
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| A new polymorphic DNA probe pS43 derived from a flow sorted library is assigned to human chromosome 20q13 |
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| A severe autosomal recessive acromesomelic dysplasia, the Hunter-Thompson type, and comparison with the Grebe type |
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| Mild hemophilia A resulting from Arg-to-Leu substitution in exon 26 of the factor VIII gene |
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| Cytogenetic analysis of in vitro fertilization (IVF) failures |
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| DNA haplotype analysis at the phenylalanine hydroxylase locus in the Turkish population |
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✓ |
|
Turkish population |
| A proposed growth regulatory function for the serologically detectable sex-specific antigen H-Ys |
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| Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndrome |
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| Hypohidrotic ectodermal dysplasia |
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| Localization of the coagulation factor XIII B subunit gene (F13B) to chromosome bands 1q31?32.1 and restriction fragment length polymorphism at the locus |
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| Detection of Duchenne muscular dystrophy carriers by dosage analysis using the DMD cDNA clone 8 |
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| Localization of Y chromosome sequences and X chromosomal replication studies in XX males |
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|
| Confirmation of linkage disequilibrium between haplotype B (XV-2c, allele 1; KM-19, allele 2) and cystic fibrosis allele in the French population |
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| Familial transmission of 16p trisomy in an infant |
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| Recombination between DXS7, DXS84 and a rare form of X-linked retinitis pigmentosa (McK-30 320) |
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| A genetic and anthropological study of atlanto-occipital fusion |
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| Ferritin H gene polymorphism in idiopathic hemochromatosis |
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| Centromeric association of a microchromosome |
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| Centromeric association and non-random distribution of centromeres in human tumour cells |
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| Chromosomal assignment of a glutamic acid transfer RNA (tRNAGlu) gene to 1p36 |
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| Chronic nonspherocytic hemolytic anemia (CNSHA) and glucose 6 phosphate dehydrogenase (G6PD) deficiency in a patient with familial amyloidotic polyneuropathy (FAP) |
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| Ataxia-telangiectasia fibroblasts have less fibronectin mRNA than control cells but have the same levels of integrin and ?-actin mRNA |
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| The human cytochrome P450 CYP3 locus: assignment to chromosome 7q22-qter |
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| H-Y antigenicity of human fibroblasts |
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| Erythrocyte acid phosphatase (ACP1) activity |
|
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| Presymptomatic testing for Huntington's disease |
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| Sublocalization of the human protein C gene on chromosome 2q13?q14 |
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| A new rare PGD variant, PGD Mediterranean |
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| The gene for the Lp(a)-specific glycoprotein is closely linked to the gene for plasminogen on chromosome 6 |
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| Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders |
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| The polymerase chain reaction: an improved method for the analysis of nucleic acids |
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| Multiple mutations underlying familial hypercholesterolemia in the South African population |
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| Erratum |
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| Prenatal diagnosis of genetic disorders in preimplantation embryos: invasive and non-invasive approaches |
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| Cystic fibrosis in Finland: a molecular and genealogical study |
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|
|
| Assignment of human desmin gene to band 2q35 by nonradioactive in situ hybridization |
|
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|
|
| BamHI and SacI RFLPs of the human immunoglobulin IGHG genes with reference to the Gm polymorphism in African people |
|
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|
✓ |
|
African people |
| Fibroblast-specific common fragile sites induced by aphidicolin |
|
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|
|
| Partial correction of chromosome instability in Fanconi anemia by desferrioxamine |
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|
| Risks of fetal cystic fibrosis based on linkage disequilibrium data |
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|
|
| Autosomal dominant polycystic kidney disease and ??4.2 thalassemia in a Caucasian family |
✓ |
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|
|
| Selection of human chromosome 21-specific DNA probes for genetic analysis in Alzheimer's dementia and Down syndrome |
|
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|
|
| Assignment of anonymous DNA probes to specific intervals of human chromosomes 16 and X |
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|
|
| A novel ?� arising from a frameshift insertion, detected by direct sequencing of enzymatically amplified DNA |
|
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|
|
| Cytogenetic investigations in a family with ataxia telangiectasia |
|
|
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|
|
| Detection of an unbalanced translocation (4;14) in a mildly retarded father and son by flow cytometry |
|
|
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|
|
|
| Detection of an alteration of the ?2 gene in a patient with chronic lung disease and serum ?2 deficiency |
|
|
|
|
|
|
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|
|
| Linkage analyses of human peptidase C (PEPC), human factor H (HF), and coagulation factor XIIIB (F13B) |
|
|
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|
|
|
|
|
|
| Announcements |
|
|
|
|
|
|
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|
|
| How does inactivation change timing of replication in the human X chromosome? |
|
|
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|
|
|
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|
|
| Long-range restriction map of a region of human chromosome 19 containing the apolipoprotein genes, a CLL-associated translocation breakpoint, and two polymorphic MluI sites |
|
|
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|
|
|
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|
|
| Molecular analysis of 46,XY females and regional assignment of a new Y-chromosome-specific probe |
|
|
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|
|
| Somatic pairing of chromosome 1 centromeres in interphase nuclei of human cerebellum |
|
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|
|
| Population bottlenecks in Polynesia revealed by minisatellites |
|
|
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|
|
| Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis |
|
|
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|
|
| Heterogeneity of mRNA expression in Italian fucosidosis patients |
|
|
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|
|
|
|
| Investigation of the ?variable spreading? of X inactivation into a translocated autosome |
|
|
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|
|
|
|
|
| The frequency and origin of the sickle cell mutation in the district of Coruche/Portugal |
|
|
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|
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|
|
|
|
| Frequency of heterozygous complete hydatidiform moles, estimated by locus-specific minisatellite and Y chromosome-specific probes |
|
|
|
|
|
|
|
|
|
| Four variants of human plasma ?2-glycoprotein (ZAG) in the Japanese population |
|
|
|
|
|
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|
|
|
| Pure partial trisomy of the short arm of chromosome 5 |
|
|
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|
|
|
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|
|
| X-Chromatin fluorescence in maternal blood |
|
|
|
|
|
|
|
|
|
| The gene encoding human low-molecular weight insulin-like growth-factor binding protein (IGF-BP25): regional localization to 7p12–p13 and description of a DNA polymorphism |
|
|
|
|
|
|
|
|
|
| Haplotype frequencies of the collagen type-I genes in the Italian population |
|
|
|
|
|
|
|
|
|
| Impairment of capping in lymphoblastoid cell lines of Duchenne patients indicates an intrinsic cellular defect |
|
|
|
|
|
|
|
|
|
| Different haplotypes for cystic fibrosis-linked DNA polymorphisms in Polish and Dutch populations |
|
|
|
|
|
|
|
|
|
| Probe walking: development of novel probes for DNA fingerprinting |
|
|
|
|
|
|
|
|
|
| Coincident maternal meiotic nondisjunction of chromosomes X and 21 without evidence of autosomal aysnapsis |
|
|
|
|
|
|
|
|
|
| Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome) |
|
|
|
|
|
|
|
|
|
| Use of variable simple sequence motifs as genetic markers: application to study of myotonic dystrophy |
|
|
|
|
|
|
|
|
|
| Human BF*F-subtypes: segregation analysis with inclusion of MHC haplotypes |
|
|
|
|
|
|
|
|
|
| Sublocalization of von Willebrand factor pseudogene to 22q11.22?q11.23 by in situ hybridization in a 46,X,t(X;22)(pter;q11.21) translocation |
|
|
|
|
|
|
|
|
|
| Correlation between chromosomal breakpoint positions and synaptic behaviour in human males heterozygous for a pericentric inversion |
|
|
|
|
|
|
|
|
|
| Chromosome abnormalities in early pregnancy analyzed by direct chromosome preparation of chorionic villi |
|
|
|
|
|
|
|
|
|
| Assignment of the gene(s) involved in the expression of the proliferation-related Ki-67 antigen to human chromosome 10 |
|
|
|
|
|
|
|
|
|
| Trisomy 18 in monozygotic twins |
|
|
|
|
|
|
|
|
|
| Deletion 3q27?3qter in an infant with mild dysmorphism, parietal meningocele, and neonatal miliaria rubra-like lesions |
|
|
|
|
|
|
|
|
|
| Detection of a rare allele with the pMP6d-9/MspI RFLP near the cystic fibrosis locus |
|
|
|
|
|
|
|
|
|
| In situ hybridization localizes the human putative oncogene GLI to chromosome subbands 12q13.3?14.1 |
|
|
|
|
|
|
|
|
|
| Haplotype analysis of familial amyloidotic polyneuropathy |
|
|
|
|
|
|
|
|
|
| Differential associative behaviour of mitotic and meiotic acrocentric chromosomes |
|
|
|
|
|
|
|
|
|
| Mapping of the gene encoding the multifunctional protein carrying out the first three steps of pyrimidine biosynthesis to human chromosome 2 |
|
|
|
|
|
|
|
|
|
| Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implications |
|
|
|
|
|
|
|
|
|
| Chromosomal localization of ARSB, the gene for human N-acetylgalactosamine-4-sulphatase |
|
|
|
|
|
|
|
|
|
| Four DNA polymorphisms in the LDL-receptor gene and their use in diagnosis of familial hypercholesterolemia |
|
|
|
|
|
|
|
|
|
| Genetics of the quantitative Lp(a) lipoprotein trait |
|
|
|
|
|
|
|
|
|
| A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosome |
|
|
|
|
|
|
|
|
|
| A hereditary double double-banded variation in the vitamin D-binding protein (GC) system analyzed by immunoblotting: duplication of the 1F and 1A2 genes? |
|
|
|
|
|
|
|
|
|
| Unbalanced translocation between chromosomes 2 and 7 with de novo deletion of band 35 on the long arm of chromosme 2 |
|
|
|
|
|
|
|
|
|
| PLG A91 and PLG M6: two new plasminogen allotypes in Japan |
|
|
|
|
|
|
|
|
|
| EcoRI RFLP in the human thyroid peroxidase (TPO) gene on chromosome 2 |
|
|
|
|
|
|
|
|
|
| Response to Wiberg's remarks on our article: ?H-Y antigenicity of human fibroblasts? |
|
|
|
|
|
|
|
|
|
| Molecular characterization of a ring chromosome 14 showing that the PI locus is centromeric to the D14S1 and IGH loci |
|
|
|
|
|
|
|
|
|
| The human cystatin C gene (CST3), mutated in hereditary cystatin C amyloid angiopathy, is located on chromosome 20 |
|
|
|
|
|
|
|
|
|
| Pregnancy-specific ?1-glycoprotein: cDNA cloning, tissue expression, and species specificity of one member of the PS?G family |
|
|
|
|
|
|
|
|
|
| Restriction analysis of chromosomal sequences homologous to single-copy fragments cloned from small polydisperse circular DNA (spcDNA) |
|
|
|
|
|
|
|
|
|
| Dose-response function for Painter's SCE-model |
|
|
|
|
|
|
|
|
|
| The factor IX BamHI polymorphism: T-to-G transversion at the nucleotide sequence-561 |
|
|
|
|
|
|
|
|
|
| Identification of a common molecular basis for combined 17?-hydroxylase/17,20-lyase deficiency in two Mennonite families |
|
|
|
|
|
|
✓ |
|
Mennonite families |
| Close linkage of MEN2A with RBP3 locus in Japanese kindreds |
|
|
|
|
|
|
|
|
|
| Specific amplification of the ZFY gene to screen sex in man |
|
|
|
|
|
|
|
|
|
| Life tables for Down syndrome |
|
|
|
|
|
|
|
|
|
| Dicarboxylic aminoaciduria associated with mental retardation |
|
|
|
|
|
|
|
|
|
| Recurrences of trisomy 18 and trisomy 13 after trisomy 21 |
|
|
|
|
|
|
|
|
|
| Renin locus restriction fragment length polymorphism |
|
|
|
|
|
|
|
|
|
| Announcements |
|
|
|
|
|
|
|
|
|
| Diagnosis of genetic disease using recombinant DNA. Second edition |
|
|
|
|
|
|
|
|
|
| Clinical and biochemical studies in three patients with severe early infantile Cockayne syndrome |
|
|
|
|
|
|
|
|
|
| Linkage analysis of hereditary thyroid carcinoma with and without pheochromocytoma |
|
|
|
|
|
|
|
|
|
| Two distinct variants of erythrocyte spectrin ?IV domain |
|
|
|
|
|
|
|
|
|
| Deletion/frameshift mutation in the ?1 null allele, PI*QObolton |
|
|
|
|
|
|
|
|
|
| Linkage disequilibrium and CF allele segregation analysis in cystic fibrosis families in Northern Ireland |
|
|
|
|
|
|
|
|
|
| TaqI polymorphism within the c-Ha-ras-1 VTR is associated with melanoma |
|
|
|
|
|
|
|
|
|
| Announcements |
|
|
|
|
|
|
|
|
|
| A new familial syndrome with impaired function of three related peptide growth factors |
|
|
|
|
|
|
|
|
|
| Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction |
|
|
|
|
|
|
|
|
|
| Evidence for male X chromosomal mosaicism in X-linked agammaglobulinemia |
|
|
|
|
|
|
|
|
|
| Genotoxic effect of benzene hexachloride in cultured human lymphocytes |
|
|
|
|
|
|
|
|
|
| Distribution of meiotic recombination along nondisjunction chromosomes 21 in Down syndrome determined using cytogenetics and RFLP haplotyping |
|
|
|
|
|
|
|
|
|
| Regional chromosomal assignment of the human glucocorticoid receptor gene to 5q31 |
|
|
|
|
|
|
|
|
|
| X-linked megalocornea: close linkage to DXS87 and DXS94 |
|
|
|
|
|
|
|
|
|
| Expression of the human ETS-2 oncogene in normal fetal tissues and in the brain of a fetus with trisomy 21 |
|
|
|
|
|
|
|
|
|
| Localization of polymorphic DNA probes frequently deleted in lung carcinoma |
|
|
|
|
|
|
|
|
|
| Heterogeneity of chromosomal breakage levels in epithelial tissue of ataxia-telangiectasia homozygotes and heterozygotes |
|
|
|
|
|
|
|
|
|
| Linkage disequilibrium for DNA haplotypes near the cystic fibrosis locus in two South European populations |
|
|
|
|
✓ |
|
|
|
South European populations |
| The human homolog of the myeloproliferative virus maps to chromosome band 1p34 |
|
|
|
|
|
|
|
|
|
| Restriction fragment length polymorphism of human aldehyde dehydrogenase 1 and aldehyde dehydrogenase 2 loci |
|
|
|
|
|
|
|
|
|
| Population cytogenetics of folate-sensitive fragile sites |
|
|
|
|
|
|
|
|
|
| Genotypes of alcohol dehydrogenase and aldehyde dehydrogenase loci in Japanese alcohol flushers and nonflushers |
|
|
|
|
|
|
✓ |
|
Japanese |
| Regional assignment of the loci for adenylate kinase to 9q32 and for ?1-acid glycoprotein to 9q31-q32 |
|
|
|
|
|
|
|
|
|
| Parental age and the origin of trisomy 21 |
|
|
|
|
|
|
|
|
|
| Physical mapping of DXS134 close to the DXS52 locus |
|
|
|
|
|
|
|
|
|
| Cytogenetic and in situ DNA-hybridization studies in intracranial tumors of a patient with central neurofibromatosis |
|
|
|
|
|
|
|
|
|
| The absence of type II collagen and changes in proteoglycan structure of hyaline cartilage in a case of Langer-Saldino achondrogenesis |
|
|
|
|
|
|
|
|
|
| DNA restriction fragment length polymorphisms in differential diagnosis of genetic disease: application in neuromuscular diseases |
|
|
|
|
|
|
|
|
|
| Non C-banding variants in some normal families might be homogeneously staining regions |
|
|
|
|
|
|
|
|
|
| The role of recombination in the evolvement of the fragile X mutation |
|
|
|
|
|
|
|
|
|
| Mapping the human ZFX locus to Xp21.3 by in situ hybridization |
|
|
|
|
|
|
|
|
|
| Localization of human platelet proteoglycan gene to chromosome 10, band q22.1, by in situ hybridization |
|
|
|
|
|
|
|
|
|
| Remarks on the article “Use of linkage equilibrium data in prenatal diagnosis of cystic fibrosis” by L. Strain et al. |
|
|
|
|
|
|
|
|
|
| Preliminary exclusion of an X-linked gene in Leber optic atrophy by linkage analysis |
|
|
|
|
|
|
|
|
|
| Mitochondrial DNA polymorphism in Finnish families with Leber's hereditary optic neuroretinopathy |
|
|
|
|
|
|
✓ |
|
Finnish |
| Interaction at clinical level between erythrocyte acid phosphatase and adenosine deaminase genetic polymorphisms |
|
|
|
|
|
|
|
|
|
| Isolation of a DNA probe of potential use for diagnosis of the fragile-X syndrome |
|
|
|
|
|
|
|
|
|
| Digoxigenated oligonucleotide probes specific for simple repeats in DNA fingerprinting and hybridization in situ |
|
|
|
|
|
|
|
|
|
| The gene coding for the p68 calcium-binding protein is localised to bands q32?q34 of human chromosome 5, and to mouse chromosome 11 |
|
|
|
|
|
|
|
|
|
| Molecular cloning of the translocation breakpoint in T-ALL 11;14 (p13;q11): genomic map of TCR alpha and delta region on chromosome 14q11 and long-range map of region 11p13 |
|
|
|
|
|
|
|
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| A rapid method for detection of Y-chromosomal DNA from dried blood specimens by the polymerase chain reaction |
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| Assignment of human aldolase C gene to chromosome 17, region cen?q21.1 |
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| Tissue specificity of chromosomal rearrangements in ataxia-telangiectasia |
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| Molecular analysis of the isochromosome 12P in the Pallister-Killian syndrome |
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| Apolipoprotein (apo) E genotypes by polymerase chain reaction and allele-specific oligonucleotide probes: no detectable linkage disequilibrium between apo E and apo CII |
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| The ? subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies |
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| Erratum |
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| Molecular defects of type III procollagen in Ehlers-Danlos syndrome type IV |
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| Genetic studies of human apolipoproteins |
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| Cytogenetic studies on three pheochromocytomas derived from patients with von Hippel-Lindau syndrome |
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| Newborn screening by DNA analysis of dried blood spots |
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| Determining informativity of marker typing for genetic counseling in a pedigree |
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| Myotonia congenita (Thomsen's disease) excluded from the region of the myotonic dystrophy locus on chromosome 19 |
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| Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13 |
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| The levels of ?, ?, and ? chains in patients with Hb H disease |
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| Amplification of satellite III DNA in an unusually large chromosome 14p+ variant |
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| Family study of common fragile sites |
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| Polyclonal hyper-immunoglobulin G1(A1) syndrome |
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| Partial trisomy of distal 8q derived from mother with mosaic 8q23.3?24.13 deletion, and relatively mild expression of trichorhinophalangeal syndrome I |
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| Use of linkage disequilibrium data in prenatal diagnosis of cystic fibrosis |
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| Sister chromatid exchange analysis of the 15q11 region in Prader-Willi syndrome patients |
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| Rejoining between 9q+ and Philadelphia chromosomes results in normal-looking chromosomes 9 and 22 in Ph1-negative chronic myelocytic leukemia |
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| Inheritance of mitochondrial aldehyde dehydrogenase: genotyping in Chinese, Japanese and South Korean families reveals dominance of the mutant allele |
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| Characterization of patients with glycerol kinase deficiency utilizing cDNA probes for the Duchenne muscular dystrophy locus |
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| Familial ring (20) chromosomal mosaicism |
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| Different Hoechst 33342 and DAPI fluorescence of the human Y chromosome in bivariate flow karyotypes |
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| Genetic polymorphism of human peptidase C, PEPC (E.C.3.4.1.1): formal genetic and population data |
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| Reply to letter by Knoll et al. |
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| Non-random aberrant breakpoints in chronic myelogenous leukaemia revisited |
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| Galactose-1-phosphate uridyl transferase in density-fractionated erythrocytes |
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| Radioresistant DNA synthesis and human genetic disease |
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| The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11 |
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| Kinetochore development in two dicentric chromosomes in man |
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| Family and population studies on the human pepsinogen A multigene family |
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| Nucleolar structures in chromosome and SC preparations from human oocytes at first meiotic prophase |
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| Brachytelephalangic chondrodysplasia punctata: a possible X-linked recessive form |
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| Demonstration of spontaneous XX/XY chimerism by DNA fingerprinting |
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| Gm and Km allotypes in 74 Chinese populations: a hypothesis of the origin of the Chinese nation |
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| Mapping studies of the serum cholinesterase-2 locus (CHE2) |
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| Increased frequencies of sister chromatid exchanges at common fragile sites (1)(q42) and (19)(q13) |
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| Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastoma |
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| Chromosomal localization of human aspartate aminotransferase genes by in situ hybridization |
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| DNA haplotypes and frameworks linked to the ?-globin locus in an Austro-Asiatic population with a high prevalence of hemoglobin E |
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✓ |
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Austro-Asiatic population |
| Regional localization of human ecto-5?nucleotidase to chromosome 6q14?q21 |
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| Cytosine methylation and the fate of CpG dinucleotides in vertebrate genomes |
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| RELP-discordance within the human phenylalanine hydroxylase locus |
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| Congenital hyperthyroidism with reciprocal translocation t(1;17)(q25;q21) |
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| On the parental origin of the deletion in Angelman syndrome |
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| Two type II keratin genes are localized on human chromosome 12 |
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| A linkage group with FRA16B (the fragile site at 16q22.1) |
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| Centromeric alpha satellite DNA amplification and translocation in an unusually large chromosome 14p+ variant |
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| Increased spindle resistance to antimicrotubule agents in cells prone to chromosomal nondisjunction |
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| An unusual translocation associated with recurrent spontaneous abortions |
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| The problem of our common mitochondrial mother |
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| Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndrome |
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| Three novel partial deletions of the low-density lipoprotein (LDL) receptor gene in familial hypercholesterolemia |
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| Fragile sites and breakpoints in constitutional rearrangements and in human sperm chromosomes |
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| A case of hereditary persistence of fetal hemoglobin caused by a gene not linked to the β-globin cluster |
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| Mapping the mutation causing the X-linked lymphoproliferative syndrome in relation to restriction fragment length polymorphisms on Xq |
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| Linkage analysis of seven kindreds with the X-linked lymphoproliferative syndrome (XLP) confirms that the XLP locus is near DXS42 and DXS37 |
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| Hungarian surveillance of germinal mutations |
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| MASA syndrome: further clinical delineation and chromosomal localisation |
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| The predictive value of chorionic villus histology for identifying chromosomally normal and abnormal spontaneous abortions |
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| Detection of ?-thalassemia and hemoglobin E genes in Thai by a DNA amplification technique |
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| Lack of complementation between xeroderma pigmentosum complementation groups D and H |
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| Frequency and molecular types of deletional α-thalassemia in Egypt |
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| Isolation and characterization of the complete human ?-myosin heavy chain gene |
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| Increase of sister chromatid exchanges in excision repair deficient xeroderma pigmentosum |
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| Regional localization of the TIMP gene on the human X chromosome |
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| Expression of fragile sites in human sperm and lymphocyte chromosomes |
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| Expression of folate-sensitive fragile sites in lymphocyte chromosomes |
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| Analysis of two 47,XXX males reveals X-Y interchange and maternal or paternal nondisjunction |
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| Til 1 ? a human lymphoblastoid cell line with minimal DNA methylation |
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| The human homologues of Fim1, Fim2/c-Fms, and Fim3, three retroviral integration regions involved in mouse myeloblastic leukemias, are respectively located on chromosomes 6p23, 5q33, and 3q27 |
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| A Pro → Leu substitution in codon 369 of the alpha-1-antitrypsin deficiency variant PI MHeerlen |
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| Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma |
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| Chromosomal assignment of two myosin alkali light-chain genes encoding the ventricular/slow skeletal muscle isoform and the atrial/fetal muscle isoform (MYL3, MYL4) |
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| A ?-thalassemia mutant caused by a 300-bp deletion in the human ?-globin gene |
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| Controversy concerning paternal age effect in 47,+21 Down's syndrome |
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| Genetic polymorphism of the apolipoprotein B gene locus influences serum LDL cholesterol level in familial hypercholesterolemia |
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| Apolipoprotein B amino acid 3611 substitution from arginine to glutamine creates the Ag (h/i) epitope: the polymorphism is not associated with differences in serum cholesterol and apolipoprotein B lev |
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| Maternal origin of a de novo chromosome 8 deletion in a patient with Langer-Giedion syndrome |
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| Chromosomal localization of human glutathione transferase genes of classes alpha, mu and pi |
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| Chromosomal characteristics of malignant lymphoma |
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| The gene for human interleukin 7 (IL7) is at 8q12-13 |
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| Is there a correlation between morphological and cytogenetic findings in placental tissue from early missed abortions? |
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| Inactivated X chromosome fold in human leukemia and related clonal disorders |
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| Tissue-specific 45,X0/47,XY,+13 mosaicism in an 18-year-old woman |
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| A new polymorphic variant of human complement factor I |
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| Gene symbols for fragile sites: a proposal |
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| Study of restriction fragment length polymorphisms at the human phenylalamine hydroxylase locus and evaluation of its potential application in prenatal diagnosis of phenylketonuria in Chinese |
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|
✓ |
|
Chinese |
| Linkage analysis of the Duffy blood group marker with several chromosome 1 genes in an extended pedigree with Charcot-Marie-Tooth disease |
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| Incontinentia pigmenti and X-autosome translocations |
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| Linkage of X-linked retinitis pigmentosa to the hypervariable DNA marker M27? (DXS255) |
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| Demonstration of a Sandhoff disease-associated autosomal 50-kb deletion by field inversion gel electrophoresis |
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| Nucleolus organizer regions (NORs) inserted in 6q15 |
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| Duplication of an Xp segment that includes the ZFX locus causes sex inversion in man |
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| Genetic polymorphism of human urine deoxyribonuclease I |
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| Remarks on the article ?H-Y antigenicity of human fibroblasts? by C. Jorgensen and E.J. Eichwald |
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| Announcements |
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| Increased detectability of somatic changes in the DNA from human tumours after probing with ?synthetic? and ?genome-derived? hypervariable multilocus probes |
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| Prenatal enzymatic diagnosis of Krabbe disease (globoid-cell leukodystrophy) using chorionic villi |
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| Why is the cystic fibrosis gene so frequent? |
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| Linkage of PGK1 to X-linked severe combined immunodeficiency (IMD4) allows predictive testing in families with no surviving male |
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| G2 chromosomal radiosensitivity in families with ataxia-telangiectasia |
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| Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia |
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| Physical fine-mapping of a deletion spanning the Norrie gene |
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| The volumes and morphology of human chromosomes in mitotic reconstructions |
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| Cytogenetic and molecular analysis of an unbalanced translocation (X;7) (q28;p15) in a dysmorphic girl |
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| Molecular characterisation of three alpha-1-antitrypsin deficiency variants: proteinase inhibitor (Pi) nullcardiff (Asp256?Val); Pi Mmalton (Phe51? deletion) and Pi I (Arg39?Cys) |
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| The gene encoding the human preproacrosin (ACR) maps to the q13-qter region on chromosome 22 |
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| Isochromosome not translocation in trisomy 21q21q |
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| Haplotype and multipoint linkage analysis in Finnish choroideremia families |
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| A search for restriction fragment length polymorphism on the human Y chromosome |
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| Human interferon gamma receptor 1 (IFNGR1) gene maps to chromosome region 6q23–6q24 |
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| Phenylketonuria: detection of a frequent haplotype 4 allele mutation |
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| Unusual chromosome 20 anomaly arising ?de novo? to give dic(20)qs |
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| Reply to letter by J. H. Robbins |
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| Three F XIIIA gene loci? |
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| Fragile sites and statistics |
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| Editorial help |
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| Announcements |
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| Localization of the active type I DNA topoisomerase gene on human chromosome 20q11.2-13.1, and two pseudogenes on chromosomes 1q23-24 and 22q11.2-13.1 |
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| Molecular basis of ?-thalassemia in Thailand: analysis of ?-thalassemia mutations using the polymerase chain reaction |
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| The spectrum of ?-thalassemia mutations in northern and northeastern Thailand |
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| Cell type-dependent difference in the distribution and frequency of aphidicolin-induced fragile sites: T and B lymphocytes and bone marrow cells |
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| DNA Fingerprinting with the oligonucleotide probe (CAC)5/(GTG)5: somatic stability and germline mutations |
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| Gene assignment of Zellweger syndrome to 7q11.23: report of the second case associated with a pericentric inversion of chromosome 7 |
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| Rate of chromosomal aberrations in prenatally detected hydrops fetalis and hygroma colli |
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| Use of transgenic mice for the characterization of human alpha 1-acid glycoprotein (orosomucoid) variants |
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| No lack of complementation for unscheduled DNA synthesis between xeroderma pigmentosum complementation groups D and H |
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| Reply to letter by M. De Braekeleer |
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