| Increased sister chromatid exchanges in human cell lines characterized by monosomy X or structural abnormalities of the X chromosome |
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| The frequency of 47,+21, 47,+18, and 47,+13 at the uppermost extremes of maternal ages: results on 56,094 fetuses studied prenatally and comparisons with data on livebirths |
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| Human genes for glutathione S-transferases |
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| Studies on chiasma frequency and distribution in two fertile men carrying reciprocal translocations; one with a t(9;10) karyotype and one with a t(Y;10) karyotype |
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| The gene in search of an identity |
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| Separation of retinoblastoma and esterase D loci in a patient with sporadic retinoblastoma and del(13)(q14.1q22.3) |
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| Origin of extra chromosome in Patau syndrome |
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| Disturbances in collagen synthesis in trisomic cells from spontaneously aborted embryos |
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| Life span elongation of Werner's syndrome fibroblasts by co-culture with origin-defective SV-40 DNA transformed cells |
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| Fanconi anaemia cells are not uniformly deficient in unhooking of DNA interstrand crosslinks, induced by mitomycin C or 8-methoxypsoralen plus UVA |
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| Relationship of the variability of the heterochromatic regions of chromosomes 1, 9, 16, and Y to some anthropometric characteristics in children with embryopathies of unknown etiology and in children |
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| ?-Globin gene deletion causes ?-thalassemia syndromes in two German families |
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| A new ?2HS-glycoprotein allele (AHS * 5 ?) in two Japanese families |
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| Partial trisomy 18 due to a maternal translocation t(9;18) |
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| Prenatal diagnosis by trophoblast sampling |
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| An aetiological study of 290 XXY males, with special reference to the role of paternal age |
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| Atypical metachromatic leukodystrophy? |
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| The beta chorionic gonadotropin-beta luteinizing gene cluster maps to human chromosome 19 |
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| Prenatal identification of a deleted Y chromosome by cytogenetics and a Y-specific repetitive DNA probe |
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| Is a gene for microcephaly located on chromosome 1? |
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| Diagnostic insonation of extra utero human placentas: No effect of lymphocytic sister chromatid exchange |
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| A study of lactose absorption capacity in twins |
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| Regional mapping of the human gene for lysosomal ?-glucosidase by in situ hybridization |
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| The isolation of a genomic clone containing the apolipoprotein CII gene and the detection of linkage disequilibrium between two common DNA polymorphisms around the gene |
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| ?-Thalassemia among sickle cell anemia patients in various African populations |
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| Mitochondrial DNA polymorphism in Japanese |
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✓ |
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Japanese |
| Conservation of the human COL1A1-TK-GAA synteny and homoeologous assignment in the African green monkey and the baboon (Cercopithecoidae) |
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| Yqs in an American family of Scottish descent |
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Scottish descent |
| Pyruvate dehydrogenase activity is not deficient in the brain of three autopsied cases with Leigh disease (subacute necrotizing encephalomyelopathy, SNE) |
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| Complementation analysis in lymphoid cells from five patients with different forms of maple syrup urine disease |
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| Reproductive outcomes of paracentric inversion carriers: Report of a liveborn dicentric recombinant and literature review |
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| Coagulation factor XIII: A useful polymorphic genetic marker |
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| DNA polymerase ? inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes |
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| A nonparametric and a parametric version of a test for the detection of the presence of a major gene applicable on data for the complete nuclear family |
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| Familial apolipoprotein CII deficiency: A preliminary analysis of the gene defect in two independent families |
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| Meiotic studies and synaptonemal complex analysis in two infertile males with a 13/14 balanced translocation |
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| Population and formal genetics of the human C81(?-?) polymorphism |
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| Estimating the Recombination frequency for the PTC-Kell linkage |
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| A de novo case of trisomy 10p: Gene dosage studies of hexokinase, inorganic pyrophosphatase and adenosine kinase |
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| New chromosomal syndrome: Miller-Dieker syndrome and monosomy 17p13 |
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| PI (?1) polymorphism in the Japanese: Confirmation of PI*M4 and description of new PI variants |
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| Comparison of expression of the fragile site at Xq27 in T and B lymphocytes |
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| The Cd technique identifies a specific structure related to centromeric function |
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| A leftward deletional ?+ thalassemia found in East Sicily in conjunction with heterozygous ?-thalassemia |
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| Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases |
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| Identical twins with deletion 16q syndrome: Evidence that 16q12.2-q13 is the critical band region |
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| Y chromosome R-bands |
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| Prenatal diagnosis of Sanfilippo disease type B |
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| Determination of aldehyde dehydrogenase phenotypes using hair roots: Re-examination |
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| Contribution of reciprocal translocations to an understanding of chromosome displacement: Inferences for studies of spatial order at metaphase |
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| Synaptonemal complex studies in a mosaic 46,XY/47,XXY male |
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| On the origin of chromosomal aberrations in human peripheral lymphocytes in vitro |
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| Heterozygous female carriers of the marker-X-chromosome: IQ estimation and replication status of fra(X)(q) |
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| The use of cloned Y chromosome-specific DNA probes for fetal sex determination in first trimester prenatal diagnosis |
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| Red cell glutathione peroxidase (GPX1) variation in Afro-Jamaican, Asiatic Indian, and Dutch populations |
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✓ |
|
Afro-Jamaican, Asiatic Indian, Dutch |
| Transferrin subtypes and variants in Germany; Further evidence for a Tf null allele |
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| Mean corpuscular hemoglobin is increased in Martin-Bell syndrome |
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| A comparative study on steroid sulfatase and arylsulfatase C in fibroblast clones from 45,X/47,XXX and 69,XXY |
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| HLA antigens, glyoxalase I, and esterase D in Hong Kong Chinese |
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✓ |
|
Hong Kong Chinese |
| The inducible fragile site on chromosome 3 |
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| Hae III restriction of DNA from three cases with nonfluorescent Y chromosomes (45XO/46XYnf) |
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| High-resolution studies in patients with aniridia-Wilms tumor association, Wilms tumor or related congenital abnormalities |
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| Human chromosome hot points |
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| Duchenne muscular dystrophy |
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| 5-Azacytidine-induced undercondensations in human chromosomes |
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| Considerations on the mechanism of differential Giemsa staining of BrdU-substituted chromosomes |
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| A ?new? low incidence red cell antigen, NFLD |
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| Anthropometric definitions of dysmorphic facial signs |
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| Unusual scarcity of restriction site polymorphism in the human thyroglobulin gene. A linkage study suggesting autosomal dominance of a defective thyroglobulin allele |
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|
| Erythrocyte phosphoglucomutase: A family study of a PGM1 deficient allele |
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|
|
| The locus for apolipoprotein CII is closely linked to the apolipoprotein E locus on chromosome 19 in man |
|
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|
|
| Cytochemical and biochemical studies on neutrophil alkaline phosphatase in parents of trisomy 21 children |
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|
| Sex chromosome positions in human interphase nuclei as studied by in situ hybridization with chromosome specific DNA probes |
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|
| Prevalence of partial deficiency of red cell triosephosphate isomerase in Germany ? a study of 3000 people |
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|
|
| Genetic polymorphism of G6PD in a Bulgarian population |
|
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|
✓ |
|
Bulgarian population |
| Ecogenetic studies in Atacame�o Indians |
|
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|
|
| Excess paternal meiotic errors in Turner syndrome: natural result of ascertainment bias |
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|
| A case of achondrogenesis type I |
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|
| The fragile site on chromosome 3 |
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| Esophageal atresia, coloboma, and clubfoot in two unrelated infants |
|
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|
|
| Announcements |
|
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|
|
|
| Announcements |
|
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|
|
| Announcements |
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|
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|
|
| Further studies on compartmentalisation of DNA-topoisomerase I in Fanconi anemia tissue |
|
|
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|
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|
|
|
|
| Localisation of genetic markers and orientation of the linkage group on chromosome 19 |
|
|
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|
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|
|
| Nonrandom distribution of methotrexate-induced aberrations on human chromosomes. Detection of further folic acid sensitive fragile sites |
|
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|
|
| Spindle microtubular dysfunction in mothers of Down syndrome children |
|
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|
|
| Intercellular NOR-AG variability in man |
|
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|
|
| Prenatal detection of an unstable ring 21 chromosome |
|
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|
|
| Population studies on human phosphoglucomutase-1 thermostability polymorphism |
|
|
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|
|
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|
|
|
| Aspects of sickle cell gene in Saudi Arabia?interaction with glucose-6-phosphate dehydrogenase deficiency |
|
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|
|
| Homozygosity for fragile site at 17p12 in a 28-year-old healthy man |
|
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|
|
| Verification of Lyon's hypothesis in fragile X carriers |
|
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|
|
| Reply to Hecht and Hecht |
|
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|
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|
|
| Genetic aspects of hemifacial microsomia |
|
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|
|
|
| Announcements |
|
|
|
|
|
|
|
|
|
| PI LBEI and PI JHOU: two new alpha-1-antitrypsin alleles |
|
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|
|
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|
|
|
| Isolation and subregional mapping of a human cDNA clone detecting a common RELP on chromosome 12 |
|
|
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|
|
| The gene for human fibroblast interferon (IFB) maps to 9p21 |
|
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|
|
| Pure monosomy and trisomy 2q24.2?q3105 due to an inv ins(7;2)(q21.2;q3105q24.2) segregating in four generations |
|
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|
|
| Two new Bf S subtypes revealed by isoelectric focusing and immunofixation |
|
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|
|
| Segregation of two independent chromosomal translocations in one family |
|
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|
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| Partial deficiency of hypoxanthine-guanine phosphoribosyltransferase with reduced affinity for PP-ribose-P in four related males with gout |
|
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|
|
| Inherited XX sex reversal in the cocker spaniel dog |
|
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|
|
| The phenotype in partial 13q trisomies, apropos of a familial (13;15)(q22;q26) translocation |
|
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|
|
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|
|
| Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome |
|
|
|
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|
|
|
|
|
| A familial paracentric inversion: A short review of the current status |
|
|
|
|
|
|
|
|
|
| Unbalanced reciprocal translocations in cases of Prader-Willi syndrome |
|
|
|
|
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|
|
| The locus for apolipoprotein E (apoE) is close to the Lutheran (Lu) blood group locus on chromosome 19 |
|
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|
|
| Harvey-ras allele deletion detected by in situ hybridization to Wilms' tumor chromosomes |
|
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|
|
| Facioscapulohumeral muscular dystrophy concentrated in the village Çullar, Nevşhir, Turkey |
|
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|
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|
|
| Analysis of the DNA replication pattern of a translocation (tX/X, qter→p221::p223→qter) chromosome in leukocyte and fibroblast cultures |
|
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|
|
|
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|
|
| Interstitial deletion of the short arm of chromosome 17 |
|
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|
|
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|
|
| Meiotic translocations in two sterile males |
|
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|
|
|
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|
|
| DNA restriction fragment length polymorphisms and heterozygosity in the human genome |
|
|
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|
|
|
|
|
|
| Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention |
|
|
|
|
|
|
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|
|
| Isochromosome 6p, a unique chromosomal abnormality in retinoblastoma: Verification by standard staining techniques, new densitometric methods, and somatic cell hybridization |
|
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|
|
|
|
|
|
|
| Genetic polymorphism of complement C6 and haplotype analysis between C6 and C7 in a Japanese population |
|
|
|
|
|
|
✓ |
|
Japanese population |
| Development and behavior of synaptonemal complexes in human spermatocytes by light and electron microscopy |
|
|
|
|
|
|
|
|
|
| The identification of a DNA polymorphism of the ? fibrinogen gene, and the regional assignment of the human fibrinogen genes to 4q26-qter |
|
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|
|
|
|
|
| The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic markers |
|
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|
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|
|
| Apolipoprotein E phenotypes and hyperlipidemia |
|
|
|
|
|
|
|
|
|
| Characterization of the distribution of sister chromatid exchange frequencies: Implications for research design |
|
|
|
|
|
|
|
|
|
| Regional localization of the human genes for S-adenosylhomocysteine hydrolase (cen?q131) and adenosine deaminase (q131?qter) on chromosome 20 |
|
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|
|
| Genetic complementation in somatic cell hybrids of cerebroside sulfatase activator deficiency and metachromatic leukodystrophy fibroblasts |
|
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|
|
|
|
|
|
| Localization of the polymorphic human calcitonin gene on chromosome 11 |
|
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|
|
|
|
|
|
| Chromosome 15 anomalies and the Prader-Willi syndrome: Cytogenetic analysis |
|
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|
|
| Banding of unfixed mitotic chromosomes in suspension after release from human lymphocytes and fibroblasts |
|
|
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|
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|
|
| Four cases of partial trisomy 4p by preferential segregation in a familial 4p/17q balanced translocation |
|
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|
|
| Clonal inheritance versus variability of rRNA gene activity in human fibroblasts |
|
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|
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|
|
| Effect of caffeine in G2 on X-ray-induced chromosomal aberrations and mitotic inhibition in ataxia telangiectasia fibroblast and lymphoblastoid cells |
|
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|
|
| Autosomal fragile sites not a current indication for prenatal diagnosis |
|
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|
|
| Compound heterozygotes in hyperphenylalaninemia |
|
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|
|
| A gene regulating the time dependence of ?-l-fucosidase concentration is closely linked with the structural gene in man |
|
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|
|
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|
|
| Further study on a BF silent allele |
|
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|
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|
|
| Chromosome 13 restriction fragment length polymorphisms |
|
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|
|
| First-trimester diagnosis on chorionic villi obtained by direct vision technique |
|
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|
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|
|
| Ethnic distribution of phenylketonuria in the north German population |
|
|
|
|
|
|
✓ |
|
north German population |
| Editorial help |
|
|
|
|
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|
|
| X-linked agammaglobulinemia and the red blood cell determinants Xg and 12E7 are not closely linked |
|
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|
|
|
|
|
|
| Fetal mortality at the time of chorionic villi sampling |
|
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|
|
|
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|
|
| Hyalinosis cutis et mucosae in siblings |
|
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|
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|
|
| Confirmation of the assignment of the gene coding for the BA-2 antigen to human chromosome 12 |
|
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|
|
|
| Announcements |
|
|
|
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|
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|
|
|
| Announcements |
|
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|
| Pericentric inversions |
|
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|
|
| HLA as a marker of the hemochromatosis gene in Sweden |
|
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|
|
| A unique electrophoretic slow-moving glucose 6-phosphate dehydrogenase variant (G6PD Asahikawa) with a markedly acidic pH optimum |
|
|
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|
|
|
|
|
|
| The mode of inheritance of psoriasis: Evidence for a major gene as well as a multifactorial component and its implication for genetic counselling |
|
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|
|
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|
|
| The phenotypic effects of small, distal Xq deletions |
|
|
|
|
|
|
|
|
|
| Announcement |
|
|
|
|
|
|
|
|
|
| Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences |
|
|
|
|
|
|
|
|
|
| Exclusion of chromosomal mosaicism in prenatal diagnosis |
|
|
|
|
|
|
|
|
|
| Osteogenesis imperfecta: a heterogeneous morphologic phenotype in cultured dermal fibroblasts |
|
|
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|
|
|
|
|
|
| DNA replication and inactivation patterns in structural abnormality of sex chromosomes |
|
|
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|
|
|
|
|
|
| Polymorphisms of human albumin gene after DNA restriction by Hae III endonuclease |
|
|
|
|
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|
|
|
|
| Heterozygous carriers for Bloom syndrome exhibit a spontaneously increased micronucleus formation in cultured fibroblasts |
|
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|
|
|
|
|
|
| Statistical evaluation of sister chromatid exchanges |
|
|
|
|
|
|
|
|
|
| A new ?2HS-glycoprotein typing by isoelectric focusing |
|
|
|
|
|
|
|
|
|
| Satellited Y chromosomes: Structure, origin, and clinical significance |
|
|
|
|
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|
|
|
|
| Persistence of chromosome rearrangements in peripheral lymphocytes from patients treated with melphalan for ovarian carcinoma |
|
|
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|
|
|
|
|
|
| Fragile (X) expression: Relationship to the cell cycle |
|
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|
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|
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|
|
| Y-Dependent polypeptides identified by two-dimensional gel electrophoresis of monozygotic X0 and XY fibroblasts |
|
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|
|
|
|
|
| A list of cloned human DNA sequences-Supplement |
|
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|
|
|
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|
|
| Ring chromosome 21 in a healthy woman with three spontaneous abortions |
|
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|
|
|
|
|
|
| Use of a chromosome 21 cloned DNA probe for the analysis of non-disjunction in Down syndrome |
|
|
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|
|
| G6PD Cagliari: A new low activity glucose 6-phosphate dehydrogenase variant characterized by enhanced intracellular lability |
|
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|
|
|
| A new form of hypertrichosis inherited as an X-linked dominant trait |
|
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|
|
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|
|
| X-inactivation patterns in lymphocytes and skin fibroblasts of three cases of X-autosome translocations with abnormal phenotypes |
|
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| Cytogenetic studies in spontaneous abortuses |
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| Linkage between late onset, dominant spinocerebellar ataxia and HLA |
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| Genetic polymorphism of mitochondrial glutamate-oxaloacetate transaminase in Japanese |
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| Premature centromere splitting in a presumptive mild form of Roberts syndrome |
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| Fragile X ?homozygosity? due to somatic crossing-over? |
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| Announcements |
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| Announcements |
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| Cystic kidneys |
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| Distal duplication 14q: Report of three cases and further delineation of the syndrome |
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| Genetic linkage between erythrokeratodermia variabilis and Rh locus |
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| Characterization of normal and mutant adenosine deaminase messenger RNAs by translation and hybridization to a cDNA probe |
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| The association of the nucleolus and the short arm of acrocentric chromosomes with the XY pair in human spermatocytes: Its possible role in facilitating sex-chromosome acrocentric translocations |
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| The two apolipoprotein loci apoA-I and apoA-IV are closely linked in man |
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| Folic acid and chromosome breakage. II. A methionine effect similar to that in fragile X expression |
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| Gene frequencies of S-adenosylhomocysteine hydrolase (SAHH) in a Japanese population |
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✓ |
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Japanese population |
| Trisomy 14 by paternal origin |
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| Apolipoprotein E phenotypes in patients with myocardial infarction |
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| Reactivity pattern of 15 HLA-Dw1 homozygous typing cells in primary mixed lymphocyte culture |
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| Familial thrombocytopenia associated with platelet autoantibodies and chromosome breakage |
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| Properties of ?-l-iduronidase in cultured skin fibroblasts from ?-l-iduronidase-deficient patients |
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| A simple method for high resolution banding of chromosomes in amniotic fluid cells |
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| Transferase-deficiency galactosemia: Immunochemical studies of the Duarte and Los Angeles variants |
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| Old and new genetics help ordering loci at the telomere of the human X-chromosome long arm |
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| Hemoglobins S and C in Upper Volta |
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| ?-Globin gene deletions associated with ?Aand ?G Philadelphiagenes in an Algerian family that includes two Hb G homozygotes |
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| Meiotic studies in two infertile males with autosomal translocations |
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| Trisomy 16q13?qter in a infant from a t (11;16)(q25;q13) translocation-carrier father |
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| Announcement |
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| Modification in publication of articles dealing with genetic polymorphisms |
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| Genetic changes in mammalian cells reminiscent of an SOS response |
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| Three new phenotypes of human red cell acid phosphatase: ACP1FA, ACP1GA, and ACP1GB |
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| A re-examination of the case for homology between the X and Y chromosomes of mouse and man |
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| Telomeric association of chromosomes in B-cell lymphoid leukemia |
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| On the development of a standard two-dimensional polypeptide map of the human X chromosome |
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| The gene for coagulation factor XIII a subunit (F13A) is distal to HLA on chromosome 6 |
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| A new X-linked dysplasia gigantism syndrome: Identical with the Simpson dysplasia syndrome? |
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| Transmission of the marker X syndrome trait by unaffected males: Conclusions from studies of large families |
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| Restriction fragment length polymorphisms at the human parathyroid hormone gene locus |
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| Familial benign hypercalcaemia (FBH; McK. No. 14598, 1983): Linkage studies in a large Dutch family |
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| Del11p13/nephroblastoma without aniridia |
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| X-Y translocation. A case report |
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| X-linked Duchenne muscular dystrophy in an unusual family with manifesting carriers |
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| Familial DiGeorge syndrome and associated partial monosomy of chromosome 22 |
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| Cytogenetic studies of familial Prader-Willi syndrome |
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| Discrete subaortic stenosis as part of a short stature syndrome |
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| Study on established lymphoid cells in maple syrup urine disease. Correlation with clinical heterogeneity |
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| Human C4 polymorphism: Pedigree analysis of qualitative, quantiative, and functional parameters as a basis for phenotype interpretations |
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| The use of distamycin A in human lymphocyte cultures |
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| Detailed cell cycle analysis in human lymphocytes; Application to ?-irradiated cells |
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| Inactivation pattern of the fragile X in heterozygous carriers |
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| Gd (+) Laguna, a new rare glucose-6-phosphate dehydrogenase variant from Brazil |
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| Compoond heterozygotes in hyperphenylalaninaemia |
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| Letters to the editors |
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| Autosomal lesions versus fragile sites |
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| X long-arm deletions. A review of non-mosaic cases studied with banding techniques |
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| Genetic mapping of the structural gene for antithrombin III to human chromosome 1 |
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| Prevalence of primary adult lactose malabsorption in three populations of northern China |
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| No marker (X) syndrome in autistic children |
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| Maternal ageing and aneuploid embryos?Evidence from the mouse that biological and not chronological age is the important influence |
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| Bleomycin-induced chromosomal aberrations and sister chromatid exchanges in Down lymphocyte cultures |
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| Isoelectric focusing studies of human red cell esterase D: Evidence for polymorphic occurrence of a new allele EsD 7 in Japanese |
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✓ |
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Japanese |
| Epidemiology of neural tube defects in Germany |
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| Regional mapping of liver type 6 phosphofructokinase isoenzyme on chromosome 21 |
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| Electrophoretic variants of blood proteins in Japanese |
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| Announcement |
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| Chromosome abnormalities and season of birth |
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| Prenatal diagnosis of cystic fibrosis by assay of amniotic fluid microvillar enzymes |
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| Chromosome assignment of two cloned DNA probes hybridizing predominantly to human sex chromosomes |
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| Identification of cells from fetal bladder epithelium in human amniotic fluid |
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| Detection of H-Y in the enzyme-linked immunosorbent assay |
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| Assignment of the gene for cystathionine ?-synthase to human chromosome 21 in somatic cell hybrids |
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| Reply to the comments by Mayerov�, M�ller, Wiberg, Wolf, and Fraccaro Hum Genet 66:110?112 |
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| Human oncogenes |
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| Chromosome studies in 496 infertile males with a sperm count below 10 million/ml |
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| Familial inv(1)(p3500q21.3) associated with azoospermia |
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| A decreasing tendency for cytogenetic abnormality in peripheral lymphocytes of retinoblastoma patients with 13q14 deletion mosaicism |
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| The use of fructose 1-phosphate to detect Hunter heterozygotes in fibroblast cultures from high-risk carriers |
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| Cytogenetic investigations in mentally retarded and normal males from 14 families with the fragile site at Xq28 |
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| Population genetics of the vitamin D binding protein (GC) subtypes in the Asian-Pacific area: Description of new alleles at the GC locus |
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| Heterochromatin and nucleolus organizer regions in cells of patients with malignant and premalignant lymphatic diseases |
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| Diagnosis of infantile and juvenile forms of GM2 gangliosidosis variant 0. residual activities toward natural and different synthetic substrates |
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| Gaucher disease: The effects of phosphatidylserine on glucocerebrosidase from normal and Gaucher fibroblasts |
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| C3 polymorphism, HLA and chronic renal failure in Spaniards |
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| Techniques for estimating genetic admixture and applications to the problem of the origin of the Icelanders and the Ashkenazi Jews |
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| Cytogenetic survey in couples with recurrent fetal wastage |
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| Steroid sulphatase in man: A non inactivated X-locus with partial gene dosage compensation |
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| Genetics of urinary pepsinogen: A new hypothesis |
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| The current state of research with peripheral tissues in Huntington disease |
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| Karyotyping and identification of human chromosome polymorphisms by single fluorochrome flow cytometry |
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| Arylsulfatase A in pseudodeficiency |
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| Non-random in vitro 7;14 translocations detected in a routine cytogenetic series. 12 Examples and their possible significance |
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| Assignment of the gene for uroporphyrinogen decarboxylase to human chromosome 1 by somatic cell hybridization and specific enzyme immunoassay |
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| Sequence of centromere separation another mechanism for the origin of nondisjunction |
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| Genetic analysis of human lymphocyte proteins by two-dimensional gel electrophoresis: |
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| Complete pachytene chromomere karyotypes of human spermatocyte bivalents |
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| A sensitive and dependable assay for distinguishing hamster and human X-linked steroid sulfatase activity in somatic cell hybrids |
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| Variability in serologically detected male antigen titer and some resulting problems: A critical review |
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| Comments on the paper by M. T. Zenzes and T. E. Reed hum genet 66:103?109 (1984) |
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| Heterocellular hereditary persistence of fetal hemoglobin (HPFH). Molecular mechanisms of abnormal ?-gene expression in association with ? thalassemia and linkage relationship with the ?-globin gene c |
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| A new glucose-6-phosphate dehydrogenase variant (G-6-PD Kalyan) found in a Koli family |
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| Meiotic configurations in female trisomy 21 foetuses |
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| Regional mapping of catalase and Wilms tumor?aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305?p1306 |
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| Assignment of human phosphoribosylglycinamide synthetase locus to region 21q221 |
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| Chromosomal abnormalities in human sperm: Comparisons among four healthy men |
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| Localization of a gene which complements branched-chain amino acid transaminase deficiency to the short arm of human chromosome 12 |
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| Restriction site polymorphism in the phosphoglycerate kinase gene on the X chromosome |
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| Synchronization of human leukemic cells: Relevance for high-resolution chromosome banding |
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| Estimation of aneuploidy levels in human spermatozoa using chromosome specific probes and in situ hybridisation |
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| Familial congenital esophageal atresia |
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| Genetic polymorphism of the seventh component of complement in a Japanese population |
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✓ |
|
Japanese population |
| Smaller autosomal C band sizes in blacks than in caucasoids |
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✓ |
|
blacks; caucasoids |
| Differential enzyme activities in human esterase D phenotypes |
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| Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8 |
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| Genetic analysis of human lymphocyte proteins by two-dimensional gel electrophoresis: |
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| Diagnostic application of first trimester trophoblast sampling in 100 pregnancies |
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| Gd(-) Gifu and Gd(-) Fukuoka. Two new variants of glucose-6-phosphate dehydrogenase found in Japan |
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| Siblings with renal tubular acidosis and nerve deafness. The first family in Japan |
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