Specific staining of human chromosomes in Chinese hamster x man hybrid cell lines demonstrates interphase chromosome territories Margit SchardinT. CremerM. Lang Original Investigations Pages: 281 - 287
Individual interphase chromosome domains revealed by in situ hybridization Laura Manuelidis Original Investigations Pages: 288 - 293
Differences between cystic fibrosis and normal cells in the degree of satellite association Yehoshua RaviaLydia AviviBoleslaw Goldman Original Investigations Pages: 294 - 300
Problems in prenatal diagnosis of the ichthyosis congenita group M. -L. ArnoldI. Anton-Lamprecht Original Investigations Pages: 301 - 311
A complex three breakpoint translocation involving chromosomes 2, 4, and 9 identified by meiotic investigations of a human male ascertained for subfertility Nina SaadallahMaj Hulten Original Investigations Pages: 312 - 320
Telomeric association in a malignant fibrous histiocytoma N. MandahlS. HeimHelena Willén Original Investigations Pages: 321 - 324
Human ferritin light chain gene sequences mapped to several sorted chromosomes R. V. LeboY. W. KanJ. Drysdale Original Investigations Pages: 325 - 328
Hunter syndrome among Ashkenazi Jews in Israel; evidence for prenatal selection favoring the Hunter allele J. ZlotogoraT. SchaapG. Bach Original Investigations Pages: 329 - 332
Simultaneous production of R-bands and either replication patterns or sister chromatid differentiation P. M. KroiselW. RosenkranzD. Schweizer Original Investigations Pages: 333 - 341
Evolutionary conservation of fragile sites induced by 5-azacytidine and 5-azadeoxycytidine in man, gorilla, and chimpanzee M. SchmidG. OttJ. M. J. C. Scheres Original Investigations Pages: 342 - 350
Pathologic and nonpathologic variants of the spectrin molecule in two black families with hereditary elliptocytosis Marie-Christine LecomteD. DhermyP. Boivin Original Investigations Pages: 351 - 357
Characterization of mitoses with sister chromatid differentiation (SCD) and consequences for the analysis of proliferation kinetics and sister chromatid exchanges in asynchronously growing cells G. SpeitSabine HaupterW. Vogel Short Communications Pages: 358 - 360
Gc types in one Indian group and one Mestizo Mexican group R. LiskerR. Pérez-BriceñoEdna Aizpuru Short Communications Pages: 361 - 362
Chromosome studies in 952 infertile males with a sperm count below 10 million/ml G. BourrouillouN. DastugueP. Colomies Short Communications Pages: 366 - 367
Prenatal diagnosis of genetically determined early manifestation of autosomal dominant polycystic kidney disease? K. ZerresM. HansmannM. Stephan Clinical Case Reports Pages: 368 - 369
High-resolution banding study of an X/4 translocation in a female with Duchenne muscular dystrophy F. SaitoA. TonomuraH. Sugita Clinical Case Reports Pages: 370 - 371
A new balanced (1;22)(p22;q13) translocation in a sterile male R. MiróM. R. CaballínJ. Egozcue Cases Observed Pages: 372 - 372
