Interchromosomal DNA-containing fibres in human cells Sissel MyhraAnton Brøgger Original Investigations Pages: 183 - 189
Chromosomal damage in chronic alcohol users Günter ObeJan Herha Original Investigations Pages: 191 - 200
The rate of sister chromatid exchanges parallel to spontaneous chromosome breakage in Fanconi's anemia and to trenimon-induced aberrations in human lymphocytes and fibroblasts K. HayashiW. Schmid Original Investigations Pages: 201 - 206
Familial translocation t(3p-;21q+) associated with both Down's and Sturge-Weber's syndrome in unbalanced state Manfred HabedankGerlinde Kampe Original Investigations Pages: 207 - 216
Power of assaying inbreeding through sampling of phenotypes and mating types Ranajit Chakraborty Original Investigations Pages: 217 - 222
Structural rearrangements associated with the Ph1 chromosome in chronic granulocytic leukaemia A. M. PotterJ. C. SharpR. J. Sokol Short Communications Pages: 223 - 228
Identification of interspecific translocation chromosomes in human-Chinese hamster hybrid cells Wim Burgerhout Short Communications Pages: 229 - 231
Partial trisomy 9q: A new syndrome Catherine TurleauJ. de GrouchyP. Borniche Short Communications Pages: 233 - 241
Prenatal diagnosis of trisomy 9 Uta FranckeKurt BenirschkeOliver W. Jones Short Communications Pages: 243 - 250
Red cell esterase-D polymorphism in the population of Tuscany Marino BargagnaRanieri DomeniciAgorasti Morali Short Communications Pages: 251 - 253
Red cell uridine monophosphate kinase polymorphism in Japanese Shoji HaradaMasataka ItohShogo Misawa Short Communications Pages: 255 - 257
Missing Y chromosome in juvenile chronic myelogenous leukemia Taru HaysJames R. HumbertCharles S. August Clinical Case Reports Pages: 259 - 264