On the significance of C2, C4, and factor B polymorphisms in disease Christian RittnerJörg Bertrams Review Articles 01 February 1981 Pages: 235 - 247
Incomplete trisomy 22 A. SchinzelW. SchmidA. Grubisic Original Investigations 01 February 1981 Pages: 249 - 262
Two familial cases with trisomy 15q dist due to a rcp(5;15)(p14;q21) M. TzanchevaM. KrachounovaZv. Damjanova Original Investigations 01 February 1981 Pages: 275 - 277
Monosomy 1pter Emilio YunisLuis QuinteroMyriam Leibovici Original Investigations 01 February 1981 Pages: 279 - 282
Retinoblastoma, gross internal malformations, and deletion 13q14→q31 Emilio YunisRuth ZuñigaEfrain Ramírez Original Investigations 01 February 1981 Pages: 283 - 286
The occurrence of the Philadelphia chromosome in essential thrombocytosis Barathur R. RajendraMing-liang LeeLeonard J. Sciorra Original Investigations 01 February 1981 Pages: 287 - 291
Mid-prophase human chromosomes. The attainment of 2000 bands Jorge J. Yunis Original Investigations 01 February 1981 Pages: 293 - 298
X-linked ocular albinism Charlotte JaegerBarrie Jay Original Investigations 01 February 1981 Pages: 299 - 304
Sister chromatid differentiation and isolabeling of chromosomes S. Ved BratRam S. VermaHarvey Dosik Original Investigations 01 February 1981 Pages: 305 - 308
Satellite association in Down's syndrome E. V. DavisonD. F. RobertsM. H. Callow Original Investigations 01 February 1981 Pages: 309 - 313
Evidence for methylation of inactive human rRNA genes in amplified regions Umadevi TantravahiW. Roy BregOrlando J. Miller Original Investigations 01 February 1981 Pages: 315 - 320
Structural differences in pericentric inversions. Application to a model of risk of recombinants A. Daniel Original Investigations 01 February 1981 Pages: 321 - 328
Human chromosomal heteromorphisms in american blacks Ram S. VermaHarvey Dosik Original Investigations 01 February 1981 Pages: 329 - 337
The investigation of late cytogenetic effects in children with acute leukaemia in long remission and off all chemotherapy D. SchulerJudit SzollárBea Bogáthy Original Investigations 01 February 1981 Pages: 339 - 344
Chromosomal investigations in epileptic children during long-term therapy with phenytoin or primidone K. J. EßerF. KotlarekE. Mühler Original Investigations 01 February 1981 Pages: 345 - 348
Screening method for prolidase deficiency Fumio EndoIchiro Matsuda Original Investigations 01 February 1981 Pages: 349 - 351
Reduction of physical assignments to a standard lod table: Chromosome 1 B. J. B. KeatsN. E. MortonD. C. Rao Original Investigations 01 February 1981 Pages: 353 - 359
Regional mapping of human chromosome 3. Assignment of a glutathione peroxidase-1 gene to 3p13→3q12 Renate JohannsmannB. HellkuhlK. -H. Grzeschik Original Investigations 01 February 1981 Pages: 361 - 363
Demonstration of astrocytes in cultured amniotic fluid cells of three cases with neural-tube defect Marion CremerMelitta SchachnerTheda Voigtländer Original Investigations 01 February 1981 Pages: 365 - 370
Triplex gene dosage effect for β-glucronidase and possible assignment to band q22 in a partial duplication 7q C. DanesinoG. GimelliMaria Ottavia Ciccone Original Investigations 01 February 1981 Pages: 371 - 373
Combined action of isoniazid and para-aminosalicylic acid in vivo on human chromosomes in lymphocyte cultures Madhuri JajuManjula JajuY. R. Ahuja Original Investigations 01 February 1981 Pages: 375 - 377
Basic defect in the expression of adenosine deaminase in ADA- SCID disease investigated through the cells of an obligate heterozygote Elly Herbschleb-VoogtPeter L. PearsonP. Meera Khan Original Investigations 01 February 1981 Pages: 379 - 386
Detection of cystic fibrosis homozygotes and heterozygotes by serum isoelectrofocusing G. B. NevinN. C. NevinG. W. Tully Original Investigations 01 February 1981 Pages: 387 - 389
An improved method of typing hair sheath cells using the PGM3 locus following starch gel electrophoresis R. M. BurgessJ. G. Sutton Original Investigations 01 February 1981 Pages: 391 - 393
Bf polymorphism. A very fast variant from Nigeria B. LarsenL. S. SalimonuW. H. Marshall Original Investigations 01 February 1981 Pages: 395 - 396
An electrophoretic study of glycolytic enzymes in a human population living at high altitude: the Aymara of northern Chile and western Bolivia Robert E. FerrellTerry BertinWilliam J. Schull Original Investigations 01 February 1981 Pages: 397 - 399
Structural anomalies of the X chromosome and inactivation center M. G. MatteiJ. F. MatteiF. Giraud Original Investigations 01 February 1981 Pages: 401 - 408
Trisomy 21 for the region 21q223: Identification by high-resolution R-banding patterns J. F. MatteiM. G. MatteiF. Giraud Clinical Case Reports 01 February 1981 Pages: 409 - 411
4p- syndrome in a girl with translocation t(1;4)(q11;p16)mat Claude StollA. PennerathCh. Lausecker Clinical Case Reports 01 February 1981 Pages: 413 - 415
Gonadal agenesis in a phenotypically normal female with positive H-Y antigen M. De MarchiC. CampagnoliA. Carbonara Clinical Case Reports 01 February 1981 Pages: 417 - 419
Trisomy 22 mechanisms H. H. PunnettM. L. Kistenmacher Letters to the Editors 01 February 1981 Pages: 421 - 421
