A detailed analysis of chromosomal changes in heritable and non-heritable retinoblastoma J. SquireBrenda L. GallieR. A. Phillips Original Investigations Pages: 291 - 301
The organization of two related subfamilies of a human tandemly repeated DNA is chromosome specific M. JeanpierreDominique WeilClaudine Junien Original Investigations Pages: 302 - 310
The human T cell antigen Leu-2 (T8) is encoded on chromosome 2 G. BrunsP. KavathasL. A. Herzenberg Original Investigations Pages: 311 - 314
Genetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiency A. BallabioG. ParentiG. Andria Original Investigations Pages: 315 - 317
αααanti-4.2 Haplotype and heterozygous β° thalassemia in a Sicilian family S. AcutoG. ButticèA. Maggio Original Investigations Pages: 318 - 320
Another family with a silent allele of properdin factor B polymorphism (BF*QO) J. BertramsG. Mauff Original Investigations Pages: 321 - 323
Cytogenetic studies using various clastogens in two patients with Werner syndrome and control individuals E. GebhartM. SchinzelK. W. Ruprecht Original Investigations Pages: 324 - 327
Genetic analysis of human lymphocyte proteins by two-dimensional gel electrophoresis I. KondoT. YamamotoH. Hamaguchi Original Investigations Pages: 328 - 332
A new α1-antitrypsin allele PI*Poki: Isoelectric focusing with immobilized pH gradients as a tool for identification of PI variants I. YuasaK. Okada Original Investigations Pages: 333 - 336
Assignment of human pepsinogen A locus to the q12-pter region of chromosome 11 Bauke ZelleA. Geurts van KesselR. R. Frants Original Investigations Pages: 337 - 340
The infantile form of sialidosis type II associated with congenital adrenal hyperplasia: Possible linkage between HLA and the neuraminidase deficiency gene Takahiko OohiraNoriyuki NagataSetsuya Naito Original Investigations Pages: 341 - 343
A mitotic recombination in Wilms tumor occurs between the parathyroid hormone locus and 11p13 A. M. RaizisD. M. BecroftA. E. Reeve Original Investigations Pages: 344 - 346
GM1 gangliosidosis: Clinical and laboratory findings in eight families Roberto GiuglianiJanice Coelho DutraDinis José Breda Original Investigations Pages: 347 - 354
Polymorphism of human C2 detected by immunoblotting Gabriele DoxiadisI. DoxiadisH. Grosse-Wilde Original Investigations Pages: 355 - 358
Chromosome study of five cancers of the prostate N. B. AtkinMarion C. Baker Original Investigations Pages: 359 - 364
Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophy D. E. WilcoxN. A. AffaraP. L. Pearson Original Investigations Pages: 365 - 375
A new syndrome in the group of euhidrotic ectodermal dysplasia Zbyslaw KopyśćKazimiera BarczykElżbieta Król Clinical Case Reports Pages: 376 - 378
Reciprocal balanced translocation of the long arm of chromosome 8 to the short arm of chromosome 7 in a woman with two spontaneous abortions H. Hatzissevastou-LoukidouA. Bouli-KalachaniS. Mantalenakis Cases Observed Pages: 379 - 379
