X chromosome constitution and the human female phenotype Eeva ThermanC. DennistonMargaret Ulber Review Articles Pages: 133 - 143
A ring 14 chromosome with deleted short arm A. P. AmaroseElizabeth DorusSonia Csaszar Original Investigations Pages: 145 - 147
A gene controlling H-Y antigen on the X chromosome U. WolfM. FraccaroH. Hameister Original Investigations Pages: 149 - 154
Induction of sister chromatid exchanges by hydroxylamine, hydrazine and isoniazid and their inhibition by cysteine G. SpeitC. WickM. Wolf Original Investigations Pages: 155 - 158
Assignment of the human gene for phosphoglycolate phosphatase to chromosome 16 R. S. SparkesT. MohandasJ. D. Shulkin Original Investigations Pages: 159 - 161
The quantitative analysis of polymorphism on human chromosomes 1, 9, 16 and Y O. A. PodugolnikovaA. P. Korostelev Original Investigations Pages: 163 - 169
Silver-Stained accessory structures on human sex chromosomes S. PathakF. F. B. Elder Original Investigations Pages: 171 - 175
Differences in the levels of UV repair and in clinical symptoms in two sibs affected by xeroderma pigmentosum Miria StefaniniWilma KeijzerFiorella Nuzzo Original Investigations Pages: 177 - 182
The effect of caffeine posttreatment of X-ray-induced chromosomal aberrations in human blood lymphocytes in vitro A. T. NatarajanG. ObeF. N. Dulout Original Investigations Pages: 183 - 189
PK3: A new chromosome enzyme marker for gene dosage studies in chromosome 15 imbalance C. JunienH. Rubinson-SkalaJ. C. Kaplan Original Investigations Pages: 191 - 196
X-linked steroid sulfatase: Evidence for different gene-dosage in males and females C. R. MüllerBeate MiglH. H. Ropers Original Investigations Pages: 197 - 199
Regional assignment of the gene locus for steroid sulfatase C. R. MüllerA. WesterveldH. H. Ropers Original Investigations Pages: 201 - 204
Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223 L. TiepoloOrsetta ZuffardiH. H. Ropers Original Investigations Pages: 205 - 206
Cold synchronization for the study of peripheral blood and bone marrow chromosomes in leukemias and other hematologic disease states Bonnie BoucherC. S. Norman Original Investigations Pages: 207 - 211
Intracellular concentrations of phenylalanine, tyrosine and α-aminobutyric acid in 13 homozybotes and 19 heterozygotes for phenylketonuria (PKU) compared with 26 normals O. ThalhammerA. PollakHelga Königshofer Original Investigations Pages: 213 - 216
Comparison of N banding and silver staining of human NORs Eileen Fleming TaylorPatricia A. Martin-DeLeon Original Investigations Pages: 217 - 219
Double one-dimensional electrophoresis of human serum transferrin: A new high-resolution screening method for genetically determined variation K. AltlandR. HacklerW. Knoche Original Investigations Pages: 221 - 231
Erythrocyte G-6-PD and 6-PGD genetic polymorphisms in South African Negroes, with a note on G-6-PD and the malaria hypothesis H. W. HitzerothK. Bender Original Investigations Pages: 233 - 242
Down's syndrome in Wallonia (South Belgium), 1971–1978: Cytogenetics and incidence L. KoulischerY. Gillerot Original Investigations Pages: 243 - 250
Heterogeneity in β0 thalassemia from Algeria: Genetic, clinical and molecular studies Mériem BelhaniF. MorléJacqueline Godet Original Investigations Pages: 251 - 257
Sibling correlations and genetic estimates for selected blood variables in French Canadian children C. BouchardA. DemirjianE. Mongeau Original Investigations Pages: 259 - 263
Cd bands and centromeric function in dicentric chromosomes Paola MaraschioOrsetta ZuffadiF. Lo Curto Short Communications Pages: 265 - 267
Linkage of genes for chronic granulomatous disease and Xg G. WolffC. R. MüllerA. Jobke Short Communications Pages: 269 - 271
Galactose-1-phosphate-uridyltransferase (E.C.2.7.7.11): A simple routine method for detecting individuals heterozygous for the silent allele Gt 0 G. SiebertJ. KömpfH. Ritter Short Communications Pages: 273 - 275
The pipette method: A new rapid technique for chromosome analysis in prenatal diagnosis Uwe Claussen Short Communications Pages: 277 - 278
A duplication-deficiency X chromosome in a girl with severe mental retardation N. SacchiL. DalpràE. Kehyayan Clinical Case Reports Pages: 279 - 281
Cerebro-costo-mandibular syndrome Katsuhiko TachibanaYoshifumi YamamotoYoshikazu Kuroki Clinical Case Reports Pages: 283 - 286