Chromosome studies in patients with congenital malformations and mental retardation B. ErdtmannF. M. SalzanoMargarete S. Mattevi Original Investigations Pages: 297 - 306
Chromosomale Instabilität bei Homo- und Heterozygotie für mikrocephalia vera W. VormittagE. Kunze-MühlM. Weninger Originalarbeiten Pages: 307 - 314
Constitutive heterochromatin and micronucleoli in the human oocyte at the diplotene stage A. StahlJ. M. LucianiR. Gagné Original Investigations Pages: 315 - 327
Satellite DNA III and alkaline Giemsa staining Erica M. BühlerTaiso TsuchimotoGerhard R. Stalder Original Investigations Pages: 329 - 333
G banding in cytogenetic study of hemoblastoses E. W. FleischmanE. L. Prigogina Original Investigations Pages: 335 - 342
Del(10)p autosomal deletion syndrome: Clinical, cytogenetic and gene marker studies Uta FranckeCarol KernahanChristy Bradshaw Short Communications Pages: 343 - 351
High amniotic fluid alpha-1-fetoprotein in a case of fetal sacrococcygeal teratoma W. SchmidJ. P. Mühlethaler Clinical Case Reports Pages: 353 - 354
Meiotic chromosome study in a human female translocation heterozygote B. Uebele-KallhardtK. Knörr Clinical Case Reports Pages: 355 - 356