DNA restriction fragment length polymorphisms and heterozygosity in the human genome David N. CooperJörg Schmidtke Review Articles Pages: 1 - 16
Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention H. Moser Review Articles Pages: 17 - 40
Maternal ageing and aneuploid embryos—Evidence from the mouse that biological and not chronological age is the important influence J. D. BrookR. G. GosdenA. C. Chandley Original Investigations Pages: 41 - 45
Isochromosome 6p, a unique chromosomal abnormality in retinoblastoma: Verification by standard staining techniques, new densitometric methods, and somatic cell hybridization Jeremy SquireRobert A. PhillipsBrenda L. Gallie Original Investigations Pages: 46 - 53
Use of a chromosome 21 cloned DNA probe for the analysis of non-disjunction in Down syndrome K. E. DaviesK. HarperR. Williamson Original Investigations Pages: 54 - 56
Bleomycin-induced chromosomal aberrations and sister chromatid exchanges in Down lymphocyte cultures K. LijimaK. MorimotoM. Hirayama Original Investigations Pages: 57 - 61
G6PD Cagliari: A new low activity glucose 6-phosphate dehydrogenase variant characterized by enhanced intracellular lability A. MorelliU. BenattiA. De Flora Original Investigations Pages: 62 - 65
A new form of hypertrichosis inherited as an X-linked dominant trait M. A. Macías-FloresD. García-CruzJ. M. Cantu Original Investigations Pages: 66 - 70
X-inactivation patterns in lymphocytes and skin fibroblasts of three cases of X-autosome translocations with abnormal phenotypes Christine M. DistecheKaren SwisshelmRoberta A. Pagon Original Investigations Pages: 71 - 76
Cytogenetic studies in spontaneous abortuses T. AndrewsW. DunlopD. F. Roberts Original Investigations Pages: 77 - 84
Linkage between late onset, dominant spinocerebellar ataxia and HLA Lene WerdelinP. PlatzL. U. Lamm Original Investigations Pages: 85 - 89
Genetic polymorphism of mitochondrial glutamate-oxaloacetate transaminase in Japanese Tasuku ToyomasuShigeki SakakibaraHideo Matsumoto Original Investigations Pages: 90 - 91
Isoelectric focusing studies of human red cell esterase D: Evidence for polymorphic occurrence of a new allele EsD 7 in Japanese I. NishigakiT. Itoh Original Investigations Pages: 92 - 95
Premature centromere splitting in a presumptive mild form of Roberts syndrome P. PetrinelliA. AntonelliB. Dallapiccola Clinical Case Reports Pages: 96 - 99
Fragile X “homozygosity” due to somatic crossing-over? R. J. M. Gardner Letter to the Editor Pages: 100 - 100
