Neue Befunde zur Struktur der Chromosomen H. G. SchwarzacherE. BielekF. Ruzicka Review Articles Pages: 125 - 135
Premeiotic and early meiotic stages in the pollen mother cells of Eremurus and in human embryonic oocytes Eeva ThermanGloria E. Sarto Original Investigations Pages: 137 - 151
A new variety of hereditary sensory neuropathy Geoffrey C. RobinsonJames E. JanJames R. Miller Original Investigations Pages: 153 - 161
Somatic stability of variant C-band heterochromatin Holger HoehnKam AuGeorge M. Martin Original Investigations Pages: 163 - 168
Elimination of nucleolus organizers in a case of 13/14 Robertsonian translocation James E. HurleyS. Pathak Original Investigations Pages: 169 - 173
Tentative evidence for 3–4 haematopoetic stem cells in man H. W. HitzerothK. BenderJ. M. P. Geerthsen Original Investigations Pages: 175 - 183
A photometric method for quantifying the polymorphisms in human acrocentric chromosomes W. SchnedlU. RoscherR. Czaker Original Investigations Pages: 185 - 191
Prenatal diagnosis of globoid cell leukodystrophy (Krabbe's disease) K. Harzer Original Investigations Pages: 193 - 196
A true microculture technique for human lymphocytes Paul I. CountrymanJohn A. Heddle Original Investigations Pages: 197 - 200
Karyological characterization of a human lymphoblastoid cell line resistant to 6-thioguanine Michihiro C. YoshidaYoshiaki Kodama Original Investigations Pages: 201 - 208
Differential chromosomal radiosensitivity within the first G1-phase of the cell cycle of early-dividing human leukocytes in vitro after stimulation with PHA Bernd BeekGünter Obe Original Investigations Pages: 209 - 218
Evidence for two additional common alleles at the PGM1 locus (Phosphoglucomutase-E.C.:2.7.5.1) P. KühnlU. SchmidtmannW. Spielmann Original Investigations Pages: 219 - 223
Duchenne muscular dystrophy G. A. DanieliM. L. MostacciuoloC. Angelini Original Investigations Pages: 225 - 231
A possible association of long Y chromosomes and fetal loss Shivanand R. PatilHerbert A. Lubs Short Communications Pages: 233 - 235
Klinefelter's syndrome and incontinentia pigmenti Bloch-Sulzberger Jürgen KunzeUlrich H. FrenzelHans-Rudolf Wiedemann Clinical Case Reports Pages: 237 - 240