Cytogenetic survey of a hospital for the mentally retarded Grant R. SutherlandAshleigh R. MurchCarole Wiseman Original Investigations Pages: 231 - 245
Segmentation of human chromosomes induced by 5-ACR (5-azacytidine) Evani Viegas-PéquignotB. Dutrillaux Original Investigations Pages: 247 - 254
Chromosomal damage in epileptics on monotherapy with carbamazepine and diphenylhydantoin J. HerhaG. Obe Original Investigations Pages: 255 - 263
Studies on frequency of Y chromatin in human sperm E. SchwingerJ. ItesBettina Korte Original Investigations Pages: 265 - 270
Hand dermatoglyphics in trisomy 4p P. MastroiacovoV. CurròB. Dallapiccola Original Investigations Pages: 271 - 276
Rapid prenatal and postnatal detection of inborn errors of propionate, methylmalonate, and cobalamin metabolism: A sensitive assay using cultured cells Huntington F. WillardLalit M. AmbaniLeon E. Rosenberg Original Investigations Pages: 277 - 283
Hereditary hemolytic anemia with erythrocyte pyrimidine 5′-nucleotidase deficiency in Spain J. L. Vives-CorronsE. Montserrat-CostaC. Rozman Original Investigations Pages: 285 - 292
G6PD lozere and trinacria-like Henri VergnesMichèle GherardiAkira Yoshida Original Investigations Pages: 293 - 298
The distribution of esterase D variants in different ethnic groups Alida Cornelia Ebeli-StruijkElisabetta M. Wurzer-FigurelliP. Meera Khan Original Investigations Pages: 299 - 306
Mitosis of maternal lymphocytes in the presence of fetal cells: Possible implication in prenatal diagnosis from fetal blood samples J. P. ChaudhuriK. D. Zang Short Communications Pages: 307 - 310
The red cell 3 phosphoglycerate kinase polymorphism J. Y. Le GallC. MubambaY. Godin Short Communications Pages: 311 - 314
“Jumping” satellites in three generations: A warning for paternity tests and prenatal diagnosis G. GimelliE. PorroOrsetta Zuffardi Short Communications Pages: 315 - 318
Partial monosomy 22 as the result of an unbalanced translocation 5:22 in a patient with cri-du-chat syndrome Margherita Cirillo SilengoGeneroso Andria Clinical Case Reports Pages: 319 - 322
Trisomy 9 associated with an enlarged 9qh segment in a liveborn Marina SeabrightNina GregsonSarah Mould Clinical Case Reports Pages: 323 - 325