On the origin of the supernumerary chromosome in autosomal trisomies — with special reference to Down's syndrome U. LangenbeckI. HansmannV. Hönig Original Investigations Pages: 89 - 102
rDNA and acrocentric chromosomes in man Ginevra GuantiGioacchino MollicaFilippo Maritato Original Investigations Pages: 103 - 107
Regional mapping of human chromosome 10: Assignment of the gene for cytoplasmic glutamate-oxaloacetate transaminase to 10q24 » qter B. HellkuhlK. -H. Grzeschik Original Investigations Pages: 109 - 112
Investigations on the frequency of chromosome aberrations in bone marrow cells of Chinese hamsters after simultaneous application of caffeine and cyclophosphamide G. RöhrbornU. Buckel Original Investigations Pages: 113 - 119
Elimination of spontaneous and chemically induced chromosome aberrations in mice during early embryogenesis A. BaslerBarbara BuselmaierG. Röhrborn Original Investigations Pages: 121 - 130
The cytogenetics of 90 patients with idiopathic mental retardation/malformation syndromes and of 90 normal subjects Carolyn Trunca Doyle Original Investigations Pages: 131 - 146
Partial trisomy 4q due to familial 2/4 translocation B. BiedermanP. Bowen Original Investigations Pages: 147 - 153
Two cases of trisomy 4p with translocation t(4p-,7q+) in several members of one family Milly AndrleA. ErlachA. Rett Original Investigations Pages: 155 - 160
The red blood cell Esterase D polymorphism in Europe and Asia R. A. CartwrightI. L. BethelD. Teasdale Original Investigations Pages: 161 - 166
Mutant forms of erythrocyte glucose 6-phosphate dehydrogenase in Ashkenazi. Description of two new variants: G6PD kirovograd and G6PD zhitomir T. L. ShatskayaK. D. KrasnopolskayaL. J. Idelson Short Communications Pages: 175 - 178
The occurrence of Hb E Saskatoon in Scotland D. TillsV. MuirH. Lehmann Short Communications Pages: 179 - 180
Parental origin of a ring 13 chromosome in a female with multiple anomalies R. Ellen MagenisHerman E. WyandtJean Macfarlane Clinical Case Reports Pages: 181 - 186
Ring chromosome 15 in child with a minor dysmorphism of phenotype Lj. RumenićI. JoksimovićM. Anaf Clinical Case Reports Pages: 187 - 188
Brachydactylia with symphalangism, probably autosomal recessive Roland WalbaumClaude HazardRoger Cordier Clinical Case Reports Pages: 189 - 192
Generalized dermal perifollicular fibromas with polyps of the colon O. P. Hornstein Clinical Case Reports Pages: 193 - 197
