Multiple tumors of the skin: Clinical, histopathological, and genetic features Ulrich Berendes Reviews Pages: 181 - 210
Zur Problematik der Bestimmung seltener Varianten des C3-Polymorphismus G. MauffH. FreisG. Pulverer Originalarbeiten Pages: 211 - 220
Cyclophosphamide-induced chromosomal aberrations in nontumorous patients Matild DobosD. SchulerGy. Fekete Original Investigations Pages: 221 - 227
Automatic chromosome processing L. J. ButlerSylvia BriddonEdna L. Jackson Short Communications Pages: 229 - 232
Etude d'une modification de l'expression du locus AB0 chez un sujet 47,XY,(?18q-)+ A. MarcelliA. BenajamJ. Lejeune Communications Brèves Pages: 233 - 241
PGM3 (PGM1, PGM2) Phenotyping in human leucocytes with a simplified method H. Werner GoeddeMargrit Stahn Short Communications Pages: 243 - 245
The polymorphism of alanine aminotransferase (EC:2.6.1.2): Densitometrical assay J. KömpfS. BissbortG. G. Wendt Short Communications Pages: 247 - 249
The polymorphism of alanine aminotransferase (EC: 2.6.1.2): Spectrophotometrical assay of GPT J. KömpfS. Bissbort Short Communications Pages: 251 - 253
Un cas d'allongement des bras longs d'un chromosome B4 par insertion [46XX:ins. (4;?)(q23;?)] Brigitte HermannChristine DistècheJ. Frederic Communications Brèves Pages: 255 - 260
Genetic variation of mannose phosphate isomerase in man H. RitterU. FriedrichsonJ. Schmitt Short Communications Pages: 261 - 261
Genetic variation of aconitate hydratase in man J. SchmittH. Ritter Short Communications Pages: 263 - 264
Genetic polymorphism of hexokinase in primates H. RitterU. FriedrichsonJ. Schmitt Short Communications Pages: 265 - 266
Tricho-rhino-phalangeal syndrome — a seldom constitutional disorder. Case report U. TheileS. RiekeG. Rompe Clinical Case Reports Pages: 267 - 269
The Ellis-van creveld syndrome in an infant Ulrike HilligHans-Georg Grundner Clinical Case Reports Pages: 271 - 274
