Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11 M. AnderssonD. C. PageA. de la Chapelle Original Investigations Pages: 2 - 7
Neuropsychological deficits in obligatory heterozygotes for metachromatic leukodystrophy Herbert KohnPaul ManowitzArthur Kling Original Investigations Pages: 8 - 12
A frequent Aγ-persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with β-thalassemia S. OttolenghiC. CamaschellaM. Pirastu Original Investigations Pages: 13 - 17
Inhibition of condensation in the late-replicating X chromosome induced by 5-azadeoxycytidine in human lymphocyte cultures T. HaafG. OttM. Schmid Original Investigations Pages: 18 - 23
Human sperm chromosome studies in a reciprocal translocation t(2;5) Cristina TempladoJoaquima NavarroJosé Egozcue Original Investigations Pages: 24 - 28
Molecular characterization of a Y;15 translocation segregating in a family Tiina AlitaloJari TiihonenAlbert de la Chapelle Original Investigations Pages: 29 - 35
DA/DAPI-Fluorescent heteromorphism of human Y chromosome M. S. LinA. ZhangA. Fujimoto Original Investigations Pages: 36 - 38
Identification of a single nucleotide change in a mutant gene for hypoxanthine-guanine phosphoribosyltransferase (HPRTAnn Arbor) Shin FujimoriYuji HidakaWilliam N. Kelley Original Investigations Pages: 39 - 43
Replication kinetics of X chromosomes in fibroblasts and lymphocytes K. S. ReddyJ. R. K. SavageD. G. Papworth Original Investigations Pages: 44 - 48
X Chromosome deletions detectable by flow cytometry in some patients with steroid sulphatase deficiency (X-linked ichthyosis) A. CookeE. F. GillardM. A. Ferguson-Smith Original Investigations Pages: 49 - 52
Mitochondrial DNA polymorphism in mitochondrial myopathy I. J. HoltA. E. HardingJ. A. Morgan-Hughes Original Investigations Pages: 53 - 57
Family resemblance for serum uric acid in a Jerusalem sample of families Y. FriedlanderJ. D. KarkY. Stein Original Investigations Pages: 58 - 63
Cystic fibrosis: screening for a DNA deletion by field inversion gel electrophoresis J. MorreauM. SinaasappelD. J. J. Halley Original Investigations Pages: 64 - 67
Detection of a new hybrid α2 globin gene among American Blacks Yuan-chao GuTadako NakatsujiTitus H. J. Huisman Original Investigations Pages: 68 - 72
Mutations for the autosomal recessive and autosomal dominant forms of polycystic kidney disease are not allelic Michèle RamsayStephen T. ReedersTrefor Jenkins Original Investigations Pages: 73 - 75
Cystic fibrosis typing with DNA probes: experience of a screening laboratory Ann HarrisCaroly QuinlanMartin Bobrow Original Investigations Pages: 76 - 79
Linkage between the loci for the Lp(a) lipoprotein (LP) and plasminogen (PLG) L. R. WeitkampS. A. GuttormsenJ. S. Schultz Original Investigations Pages: 80 - 82
Variation in spontaneous chromosomal damage as a function of biologic rhythms in women Doris D'SouzaI. M. ThomasB. C. Das Short Communications Pages: 83 - 85
Characterization of a partial deletion of the factor VIII gene in a haemophiliac with inhibitor B. BardoniM. SampietroG. Camerino Short Communications Pages: 86 - 88
The tyrosinase-positive oculocutaneous albinism locus is not linked to the β-globin locus in man R. A. HeimD. S. DunnT. Jenkins Short Communications Pages: 89 - 89
G6PD Huntsville: a new glucose-6-phosphate dehydrogenase associated with chronic hemolytic anemia Kelley HallMarshall T. SchreederJosef T. Prchal Short Communications Pages: 90 - 91
Deletion 2q31.3→2q33.3: gene dosage effect of ribulose 5-phosphate 3-epimerase Bruno DallapiccolaGiuseppe NovelliAldo Giannotti Case Observed Pages: 92 - 92
