Minor chromosome variations and selected heteromorphisms in 200 unclassifiable mentally retarded patients and 200 normal controls Avirachan T. TharapelRobert L. Summitt Original Investigations Pages: 121 - 130
The fate of DNA statellites I, II, III and ribosomal DNA in a familial dicentric chromosome 13:14 J. R. GosdenChristine GosdenA. R. Mitchell Original Investigations Pages: 131 - 141
Chromosome abnormalities and clinical and morphologic manifestations of chronic myeloid leukemia E. L. PrigoginaE. W. FleischmanM. A. Frenkel Original Investigations Pages: 143 - 156
Kinetics of 21-trisomic lymphocytes A. SerraE. ArpaiaR. Bova Original Investigations Pages: 157 - 167
Reliable detection of cystic fibrosis in skin-derived fibroblast cultures Peter HösliEsther Vogt Original Investigations Pages: 169 - 173
Lack of association between psoriasis vulgaris and red cell acid phosphatase polymorphism Gila MatthaeiU. Langenbeck Original Investigations Pages: 175 - 179
Evidence for the inheritance of silver-stained nucleolus organizer regions V. D. MarkovićR. G. WortonJ. M. Berg Original Investigations Pages: 181 - 187
Evaluation of Genetic Consultations in the public health service N. P. BochkovS. I. Kozlova Original Investigations Pages: 189 - 195
Common and uncommon immunoglobulin haplotypes among Lebanese communities Gérard LefrancLiliane RivatErna van Loghem Original Investigations Pages: 197 - 209
Longueur du chromosome Y, intelligence et comportement dans une population de médico-légaux M. BénézechB. NoëlA. Mouget Short Communications Pages: 211 - 216
Centromere inactivation in a case of turner variant with two dicentric iso-long arm Y chromosomes W. SchmidV. D'Apuzzo Short Communications Pages: 217 - 223
45,X/47,XYY mosaicism in a patient with Turner's syndrome Rubén LiskerLizbeth RuzOsvaldo Mutchinick Clinical Case Reports Pages: 231 - 233
Partial trisomy 10p in two generations I. W. LurieG. I. LazjukI. A. Shved Clinical Case Reports Pages: 235 - 241
