Frequency of 9qh+ and risk of chromosome aberrations in the progeny of individuals with 9qh+ Johannes NielsenUrsula FriedrichEva Zeuthen Original Investigations Pages: 211 - 216
Ribosomal DNA sites in a metacentric chromosome fragment Leslie D. JohnsonRuth C. HarrisAnn S. Henderson Original Investigations Pages: 217 - 219
Fluorescence banding pattern of human and mouse chromosomes with a benzimidazol derivative (hoechst 33258) T. RaposaA. T. Natarajan Original Investigations Pages: 221 - 226
On the relevance of non-histone proteins to the production of Giemsa banding patterns on chromosomes W. VogelJ. FaustJ.-W. Siebers Original Investigations Pages: 227 - 236
Ein Fall von XX/XY-Chimärismus mit normalem männlichen Habitus Karl SperlingRudolf KadenWilhelm Weise Originalarbeiten Pages: 237 - 244
Ein Beitrag zur Genese von XX-Männern M. Bartsch-SandhoffH. SchadeW. Scholz Originalarbeiten Pages: 245 - 253
Down's syndrome in twins with discordant HL-A phenotypes W. HirschK. BenderG. Tariverdian Original Investigations Pages: 255 - 262
Comparative studies on the distribution of aberrations on human chromosomes treated with busulphan in vivo * and in vitro Erich Gebhart Original Investigations Pages: 263 - 272
Cross-reactions between human and animal plasma proteins Klausdieter Bauer Original Investigations Pages: 273 - 278
The formation of the abnormal chromosome in balanced homologous Robertsonian translocation carriers R. J. M. GardnerM. I. ParslowA. M. O. Veale Short Communications Pages: 279 - 282
Familial short arm deletion of chromosome No. 15 J. J. HooU. HilligF. Hermann Short Communications Pages: 283 - 286
A family with congenital pulmonary valve stenosis Timothy J. David Short Communications Pages: 287 - 288