Further delineation of the clinical picture of trisomy for the distal segment of chromosome 13 A. SchinzelK. HayashiW. Schmid Original Investigations Pages: 1 - 12
Origin of the extra chromosome No. 21 in Down's syndrome P. WagenbichlerW. KillianW. Schnedl Original Investigations Pages: 13 - 16
Maternal and paternal origin of extra chromosome in trisomy 21 Margareta MikkelsenAnni HallbergHanne Poulsen Original Investigations Pages: 17 - 21
Genetics of the +p9 syndrome I. W. LurieG. I. LazjukS. S. Usoev Original Investigations Pages: 23 - 33
A test for heterozygocity of 21-hydroxylase deficiency J. HomokiW. M. TellerA. T. A. Fazekas Original Investigations Pages: 35 - 41
Distribution of alpha-1-antitrypsin phenotypes in two Dutch population groups J. J. M. L. HoffmannW. G. M. van den Broek Original Investigations Pages: 43 - 48
Comparative studies on the specificity of anticlastogenic action in human lymphocytes in culture Erich GebhartReinhard Becher Original Investigations Pages: 49 - 64
Association of duffy blood groups with the suckle cell trait A. P. GelpiM. C. King Original Investigations Pages: 65 - 68
Epidermolysis bullosa dystrophica dominans (Pasini)—A primary structural defect of the anchoring fibrils Ingrun Anton-LamprechtIsao Hashimoto Original Investigations Pages: 69 - 76
Conduite antisociale et longueur du chromosome Y M. BenezechB. NoëlJ. Mottet Short Communications Pages: 77 - 80
Esterase D polymorphism: Description of the “new” allele EsD4 Konrad BergFreidrich SchwarzfischerHans Wischerath Short Communications Pages: 81 - 83
A note on suxamethonium sensitivity and serum cholinesterase variants D. P. AgarwalL. M. SrivastavaH. W. Goedde Short Communications Pages: 85 - 88
Short arm deletion of an X chromosome, 46,XXp- P. KaiserB. ZabelE. Daume Clinical Case Reports Pages: 89 - 100
Partial trisomy 2q and familial translocation t(2;12)(q31;q24) Bernhard ZabelSusanne HansenWolfram Hartmann Clinical Case Reports Pages: 101 - 104