Genetic disorders presenting as “schizophrenia”. Karl bonhoeffer's early view of the psychoses in the light of medical genetics P. Propping Review Articles Pages: 1 - 10
Towards an understanding of the molecular mechanisms regulating gene expression during diploidization in phylogenetically polyploid lower vertebrates M. Leipoldt Review Articles Pages: 11 - 18
Incidence at birth of different types of limb reduction abnormalities in Hungary 1975–1977 Mária BodA. CzeizelW. Lenz Original Investigations Pages: 27 - 33
Family study of congenital limb reduction abnormalities in Hungary 1975–1977 A. CzeizelMária BodW. Lenz Original Investigations Pages: 34 - 45
Cytogenetic investigation of 103 patients with primary or secondary amenorrhea O. OpitzI. HansmannB. Hinney Original Investigations Pages: 46 - 47
Chromosome anomalies in 136 couples with a history of recurrent abortions U. DiedrichI. HansmannH. -D. Probeck Original Investigations Pages: 48 - 52
On the genetic length of the short arm of the human X chromosome H. -H. RopersP. WieackerR. Williamson Original Investigations Pages: 53 - 55
The genetic basis of non-disjunction: Increased incidence of hyperploidy in oocytes from F1 hybrid mice I. HansmannJ. Jenderny Original Investigations Pages: 56 - 60
Acrosin and the acrosome in human spermatogenesis Sibylle Flörke-GerloffEdda Töpfer-PetersenW. Engel Original Investigations Pages: 61 - 67
Genetics of human S-adenosylhomocysteine hydrolase. A new polymorphism in man S. BissbortK. BenderK. H. Grzeschik Original Investigations Pages: 68 - 71
Evidence that the Menkes locus maps on proximal Xp T. F. WienkerP. WieackerH. H. Ropers Short Communications Pages: 72 - 73
Genetic counseling in families with spinal muscular atrophy type Kugelberg-Welander K. ZerresT. Grimm Short Communications Pages: 74 - 75
Manifestation of the fragile site Xq27 in fibroblasts G. BarbiP. SteinbachW. Vogel Short Communications Pages: 76 - 78
A search for linkage in families with fragile sites J. C. MulleyCatherine NichollsG. R. Sutherland Short Communications Pages: 79 - 81
Reduced NOR association frequency in a 13/18 translocation chromosome. A family study P. van TuinenLouise C. StrongS. Pathak Short Communications Pages: 82 - 84
Loss of electron-dense lamellar material from Fabry's disease fibroblasts after enzyme replacement R. N. SifersJ. S. MayesR. E. Nordquist Short Communications Pages: 85 - 87
A fragile X suppressor in the normal human blood? D. SoudekMary Emanuel Short Communications Pages: 88 - 89
