Chromosome abnormalities and season of birth P. VidebechJ. Nielsen Original Investigations Pages: 221 - 231
Apolipoprotein E phenotypes and hyperlipidemia G. UtermannI. KindermannA. Steinmetz Original Investigations Pages: 232 - 236
Apolipoprotein E phenotypes in patients with myocardial infarction G. UtermannA. HardewigF. Zimmer Original Investigations Pages: 237 - 241
Reactivity pattern of 15 HLA-Dw1 homozygous typing cells in primary mixed lymphocyte culture E. M. SchneiderU. KruppCh. Rittner Original Investigations Pages: 242 - 247
Prenatal diagnosis of cystic fibrosis by assay of amniotic fluid microvillar enzymes D. J. H. BrockD. BedgoodCaroline Hayward Original Investigations Pages: 248 - 251
Familial thrombocytopenia associated with platelet autoantibodies and chromosome breakage F. M. HelmerhorstD. C. HeatonA. T. Natarajan Original Investigations Pages: 252 - 256
Chromosome assignment of two cloned DNA probes hybridizing predominantly to human sex chromosomes Gudrun A. RappoldT. CremerH. J. Cooke Original Investigations Pages: 257 - 261
Identification of cells from fetal bladder epithelium in human amniotic fluid Harriet von KoskullP. AulaI. Virtanen Original Investigations Pages: 262 - 267
Properties of α-l-iduronidase in cultured skin fibroblasts from α-l-iduronidase-deficient patients S. FujibayashiR. MinamiS. Tsugawa Original Investigations Pages: 268 - 272
A simple method for high resolution banding of chromosomes in amniotic fluid cells Petra JägerClaudia Kuhn-Schlage Original Investigations Pages: 273 - 277
Detection of H-Y in the enzyme-linked immunosorbent assay Claire-Michele FarberDaniel LiebenthalCharlotte Cunningham-Rundles Original Investigations Pages: 278 - 279
Characterization of the distribution of sister chromatid exchange frequencies: Implications for research design Betsy HirschM. McGueJ. Cervenka Original Investigations Pages: 280 - 286
Transferase-deficiency galactosemia: Immunochemical studies of the Duarte and Los Angeles variants M. W. AndersenV. P. WilliamsR. S. Sparkes Original Investigations Pages: 287 - 290
Assignment of the gene for cystathionine β-synthase to human chromosome 21 in somatic cell hybrids Flemming SkovbyNatalie KrassikoffUta Francke Original Investigations Pages: 291 - 294
Old and new genetics help ordering loci at the telomere of the human X-chromosome long arm M. PurrelloR. NussbaumM. Siniscalco Original Investigations Pages: 295 - 299
Hemoglobins S and C in Upper Volta D. LabieC. RichinR. L. Nagel Original Investigations Pages: 300 - 302
α-Globin gene deletions associated with αAand αG Philadelphiagenes in an Algerian family that includes two Hb G homozygotes F. MorleP. JaccoudJ. Godet Original Investigations Pages: 303 - 307
Meiotic studies in two infertile males with autosomal translocations Miroslava MićićSava Mićić Clinical Case Reports Pages: 308 - 310
Trisomy 16q13→qter in a infant from a t (11;16)(q25;q13) translocation-carrier father K. HatanakaM. OzakiH. Fujita Clinical Case Reports Pages: 311 - 315
