Trisomy 10p due to a de novo t(10p;13p) V. AllerJ. A. AbrisquetaM. L. de Torres Original Investigations Pages: 129 - 134
Trisomy 12p syndrome Ikuko KondoHideo HamaguchiTadashi Haneda Original Investigations Pages: 135 - 140
A case of trisomy 3q21→qter syndrome Ikuko KondoTakeki HiranoHitoshi Takita Original Investigations Pages: 141 - 147
Translocation C:D involving chromosomes 11 and 14 M. H. CallowA. R. BoonE. V. Davison Original Investigations Pages: 149 - 153
An azoospermic male with a Y/Autosome translocation I. Lopez PajaresA. DelicadoC. Cuadrado Original Investigations Pages: 155 - 158
A woman carrier of two apparently unrelated reciprocal translocations G. SimoniE. MontaliF. Lo Curto Original Investigations Pages: 159 - 162
Incidence of major chromosome aberrations in 12,319 newborn infants in Tokyo Makoto HigurashiKumiko IijimaNobuo Watanabe Original Investigations Pages: 163 - 172
A new chromosome anomaly in acute lymphoblastic leukemia (ALL) H. Van den BergheG. DavidR. Eeckels Original Investigations Pages: 173 - 180
Genetic linkage relations of the sixth component of complement (C6) J. H. OlvingB. OlaisenP. Teisberg Original Investigations Pages: 181 - 192
Inhibition of condensation of human Y chromosome by the fluorochrome Hoechst 33258 in a mouse-human cell hybrid Menashe MarcusAlona NattenbergAlfred Gropp Original Investigations Pages: 193 - 198
Clinical and biochemical investigations on patients with partial deficiency of placental steroid sulfatase H. HameisterG. WolffH. H. Ropers Original Investigations Pages: 199 - 207
Variability of bacterial gene-directed enzyme production in human genetically deficient cells Jürgen HorstFriedrich KlugeWolfgang Gerok Original Investigations Pages: 209 - 217
‘GPI Roma’, a new glucose phosphate isomerase deficient variant G. IsacchiD. CottreauA. Kahn Original Investigations Pages: 219 - 226
Partial duplication of the short arm of chromosome 9 (p13→p22) in a child with typical 9p trisomy phenotype J. P. FrynsP. CasaerH. Van den Berghe Clinical Case Reports Pages: 231 - 235
Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission karyotype: 46,XX,-13,+t(13;13)(p11;q11)/46,XX,del(13)(p11) J. P. FrynsP. CasaerH. Van den Berghe Clinical Case Reports Pages: 237 - 241