Molecular evidence for true isochromosome 21q Jean H. PriestR. Dwain BlackstonStephen T. Warren Original Investigations Pages: 1 - 3
Lesch-Nyhan syndrome: molecular investigation of three French Canadian families using a hypoxanthine-guanine phosphoribosyltransferase cDNA probe Daniel SinnettLéo LavergneDamian Labuda Original Investigations Pages: 4 - 8
Effects of folate in culture medium on common fragile sites in lymphocyte chromosomes from normal and leukemic children Richard J. GreenDonald L. PhillipsAbdel H. Ragab Original Investigations Pages: 9 - 12
Molecular studies of haemophilia B in Sweden Claes WadeliusMargareta BlombäckUlf Pettersson Original Investigations Pages: 13 - 17
Molecular characterization of ataxia telangiectasia T cell clones Marc-Henri SternFangrong ZhangAlain Aurias Original Investigations Pages: 18 - 22
A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphisms B. BardoniS. GuioliG. Camerino Original Investigations Pages: 23 - 25
A family study of multiple mutations of alpha and delta glycophorins (glycophorins A and B) C. -H. HuangK. V. PugliaO. O. Blumenfeld Original Investigations Pages: 26 - 30
Variability of human rRNA genes: inheritance and nonrandom chromosomal distribution of structural variants of nontranscribed spacer sequences I. V. GarkavtsevT. G. TsvetkovaA. V. Gudkov Original Investigations Pages: 31 - 37
Increased methotrexate-induced chromosome breakage in patients with free trisomy 21 and their parents Lothar PelzJürgen GötzGabriele Witt Original Investigations Pages: 38 - 40
Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours M. MannensR. M. SlaterP. L. Pearson Original Investigations Pages: 41 - 48
Isolation of human chromosome 21 sequences and their application to in situ hybridization Kong H. ChooGay FilbyRuth Brown Original Investigations Pages: 49 - 53
Cystic fibrosis: typing 89 German families with linked DNA probes J. WeberC. Aulehla-ScholzK. Olek Original Investigations Pages: 54 - 56
Molecular evidence that the esterase-D gene lies proximal to the retinoblastoma susceptibility locus in chromosome region 13q14 Christopher D. MitchellJohn K. Cowell Original Investigations Pages: 57 - 60
Spondyloepiphyseal dysplasia tarda: linkage with genetic markers from the distal short arm of the X chromosome S. Szpiro-TapiaA. SefianiM. C. Hors-Cayla Original Investigations Pages: 61 - 63
Family studies in scleroderma (systemic sclerosis) demonstrating an HLA-linked increased chromosomal breakage rate in cultured lymphocytes Gabriele RittnerGesa SchwanitzChristian Rittner Original Investigations Pages: 64 - 70
Klinefelter's syndrome in Sardinia and Scotland Andrew D. CarothersGiorgio Filippi Original Investigations Pages: 71 - 75
DNA haplotypes of the human apoprotein B gene in coronary atherosclerosis G. A. A. FernsD. RobinsonD. J. Galton Original Investigations Pages: 76 - 80
A mosaic 45,X/46,X,4(?) karyotype investigated with X and Y centromere-specific probes using a non-autoradiographic in situ hybridization technique J. A. CrollaJ. C. Llerena Jr. Original Investigations Pages: 81 - 84
Linkage studies in X-linked Alport's syndrome S. Szpiro-TapiaG. BobrieM. C. Hors-Cayla Original Investigations Pages: 85 - 87
Assignment of ecto-5′-nucleotidase to human chromosome 6 J. M. BoyleY. HeyM. Fox Original Investigations Pages: 88 - 92
Genetic studies of low-abundance human plasma proteins M. I. KambohL. LyonsR. E. Ferrell Short Communications Pages: 93 - 94
A new method for FXIIIA genetic variants determination using isoelectric focusing in 1 M urea Ismail M. Sebetan Short Communications Pages: 95 - 97
