Sister chromatid exchanges and heterochromatin Ingo SchubertRigomar Rieger Review Articles Pages: 119 - 130
Pericentric inversions of chromosome 12 in two families F. PrietoL. BadíaM. -J. Figuera Original Investigations Pages: 131 - 133
Detection of G-C rich heterochromatin by 5-azacytidine in mammals Evani Viegas-PéquignotBernard Dutrillaux Original Investigations Pages: 134 - 137
The genes for growth hormone and chorionic somatomammotropin are on the long arm of human chromosome 17 in region q21→qter Donna L. GeorgeJohn A. Phillips IIIPeter H. Seeburg Original Investigations Pages: 138 - 141
Gene dosage effect for GALT in 9p trisomy and in 9p tetrasomy with an improved technique for GALT determination P. EydouxC. JunienC. Gregori Original Investigations Pages: 142 - 144
Arthrogryposis-like signs in trisomy 18 J. C. LambertM. FerrariR. Mariani Original Investigations Pages: 145 - 147
The “Cat Eye syndrome”: Dicentric small marker chromosome probably derived from a No. 22 (Tetrasomy 22pter→q11) associated with a characteristic phenotype A. SchinzelW. SchmidRoberta A. Pagon Original Investigations Pages: 148 - 158
The turner phenotype and the different types of human X isochromsome Priscila G. OttoAngela M. Vianna-MorganteAnita Wajntal Original Investigations Pages: 159 - 164
Multiple cytogenetically abnormal clones in two polycythemia vera patients Joseph R. TestaJeffrey R. KanofskyJoseph M. Baron Original Investigations Pages: 165 - 168
A radioenzymatic assay of catechol-O-methyltransferase in hair root cells: Comparison with erythrocyte activity J. J. HooT. StrohmeyerH. W. Goedde Original Investigations Pages: 169 - 171
Search for a relationship between molecular anomalies of the mutant erythrocyte pyruvate kinase variants and their pathological expression Axel KahnJoelle MarieAlbert Najman Original Investigations Pages: 172 - 175
Distribution of α1-(PI) phenotypes in chromosome abnormalities John C. MulleyGrant R. Sutherland Original Investigations Pages: 176 - 179
Distances électrophorétiques entre l'Homme, le Chimpanzé (Pan troglodytes) et le Gorille (Gorilla gorilla) basées sur la mobilité des enzymes érythrocytaires G. LucotteJ. Lefebvre Original Investigations Pages: 180 - 184
HGPRT structural gene mutation in Lesch-Nyhan-syndrome as indicated by antigenic activity and reversion of the enzyme deficiency Michael StraussLieselotte LübbeErhard Geissler Original Investigations Pages: 185 - 188
Phenotypic interaction studies of HPRT mutant and normal human fibroblasts I. WillersS. SinghH. W. Goedde Original Investigations Pages: 189 - 191
The genetic structure of the Kuwaiti population Khaled E. Al-NassarP. Michael ConneallyPao-lo Yu Original Investigations Pages: 192 - 198
Chromosome banding and compaction A. Leth BakA. Lund JørgensenJ. Zeuthen Short Communication Pages: 199 - 202
Lack of position effect on the activity of SODCu/Zn gene in subjects with 21/D and 21/G robertsonian translocations N. CrostiA. RigoA. Serra Short Communication Pages: 203 - 204
Further evidence against linkage between christ-siemens-touraine (CST) and XG loci E. A. Chautard-Freire-MaiaS. L. Primo-ParmoN. Freire-Maia Short Communication Pages: 205 - 206
Ring (15) chromosome Emilio YunisMyriam LeiboviciLuis Quintero Clinical Case Reports Pages: 207 - 209
Partial monosomy 7q syndrome due to distal interstitial deletion Richard StallardRichard C. Juberg Clinical Case Reports Pages: 210 - 213
Interstitial deletion (2)(p13p15) Daniela DucaDoina IoanC. Maximilian Clinical Case Reports Pages: 214 - 216
Heritable fragile sites on human chromosomes Grant R. SutherlandLynene Hinton Clinical Case Reports Pages: 217 - 219
Serial duplication of 10 (q21→q22) in a mentally retarded boy with congenital malformations Maila KoivistoRiitta HervaSirkka-Liisa Linna Clinical Case Reports Pages: 224 - 225
Combined erythrocyte glucosephosphate isomerase (GPI) and glucose-6-phosphate dehydrogenase (G6PD) deficiency in an italian family H. ArnoldG. W. LöhrR. Ludwig Clinical Case Reports Pages: 226 - 229