Sequence of centromere separation: Analysis of mitotic chromosomes in man Baldev K. Vig Original Investigations Pages: 247 - 252
A deletion in chromosome 22 can cause digeorge syndrome Albert de la ChapelleRiitta HervaPertti Aula Original Investigations Pages: 253 - 256
Observations on the effect of X-ray alone and in combination with ultrasound on human chromosomes E. Kunze-Mühl Original Investigations Pages: 257 - 260
Symmetrical replication patterns and sex chromatin bodies formation of an idic(X)(p22.3::p22.3) chromosome O. MutchinikL. CasasO. Lozano Original Investigations Pages: 261 - 264
H-Y antigen negative patients with testicular tissue and 46,XY karyotype F. P. HaseltineM. GenelW. R. Breg Original Investigations Pages: 265 - 268
Effects of radical-scavenging enzymes and reduced oxygen exposure on growth and chromosome abnormalities of Werner syndrome cultured skin fibroblasts D. SalkK. AuG. M. Martin Original Investigations Pages: 269 - 275
Population screening for the human adult lactase phenotypes with a multiple breaths version of the breath hydrogen test J. N. HowellT. SchockenhoffG. Flatz Original Investigations Pages: 276 - 278
Distribution of the lactase phenotypes in the population of the Democratic Republic of the Sudan R. A. L. BayoumiN. SahaG. Flatz Original Investigations Pages: 279 - 281
Studies on complementation in argininosuccinate synthetase and argininosuccinate lyase deficiencies in human fibroblasts Liliane CathelineauDanielle Pham DinhPierre Kamoun Original Investigations Pages: 282 - 284
Zum praktischen Wert des Lymphozytenmodells für die pathogenetische Beurteilung einzelner Serumcholesterinfraktionen des Menschen bei der autosomal-monogenen Hypercholesterinämie Th. WichmannH. -A. FreyeK. Berndt Original Investigations Pages: 285 - 289
Defining the locus of origin of a genetically determined electrophoretic variant of a multilocus enzyme system; the calcutta-1 of human LDH system is a B-locus variant Elly Herbschleb-VoogtP. Meera Khan Original Investigations Pages: 290 - 295
Reduced uptake and incorporation of 3H-thymidine in fanconi anemia fibroblasts M. ShoyabM. GunnellA. S. Lubiniecki Original Investigations Pages: 296 - 299
Aniridia, male pseudohermaphroditism, gonadoblastoma, mental retardation, and del 11p13 Catherine TurleauJ. de GrouchyNicole Diebold Original Investigations Pages: 300 - 306
Inheritance and genetic linkage of transcobalamin II Soo Young YangPeter ColemanBo Dupont Original Investigations Pages: 307 - 311
Gc revisited: Six further Gc-phenotypes delineated by isoelectric focusing and by polyacrylamide gel electrophoresis H. CleveJ. ConstansW. Weber Original Investigations Pages: 312 - 316
Linkage of GLO with HLA in a sample of the Spanish population C. Lopez-LarreaA. BootelloA. Arnaiz-Villena Original Investigations Pages: 317 - 320
Chromosome-damaging action of isoniazid and thiacetazone on human lymphocyte cultures in vivo Y. R. AhujaMadhuri JajuManjula Jaju Short Communications Pages: 321 - 322
Use of genetic markers to certify fetal origin of cultured amniotic fluid cells Shi-Han ChenL. E. KarpW. Chen Short Communications Pages: 323 - 324
Adenylate kinase deficiency and malignant hyperthermia C. G. CerriJ. H. WillnerD. S. Wood Short Communications Pages: 325 - 326
Alpha-1-antitrypsin (Pi) types in Korean and Chinese populations Chung Choo LeeF. KueppersG. Rodgers Short Communications Pages: 327 - 328
Acute lymphocytic and myelomonocytic leukemia associated with low platelet counts and a 21q- marker chromosome Giuliana AlimenaBruno DallapiccolaFelix Mitelman Clinical Case Reports Pages: 329 - 331
Gd(-) Muret and Gd(-) Colomiers, two new variants of glucose-6-phosphate dehydrogenase associated with favism H. VergnesA. RibetH. Brun Clinical Case Reports Pages: 332 - 334
