Evolution of the Simiiformes and the phylogeny of human chromosomes I. C. ClementeM. PonsàJ. Egozcue Review Article Pages: 493 - 506
Microdissection of banded human chromosomes Gabriele SengerHermann-Josef LüdeckeUwe Claussen Original Investigations Pages: 507 - 511
Construction and characterization of band-specific DNA libraries Hermann-Josef LüdeckeGabriele SengerBernhard Horsthemke Original Investigations Pages: 512 - 516
Cocultivation of Fanconi anemia cells and of mouse lymphoma mutants leads to interspecies complementation of chromosomal hypersensitivity to DNA cross-linking agents Filippo RosselliEthel Moustacchi Original Investigations Pages: 517 - 521
Segregation analysis of 1885 DMD families: significant departure from the expected proportion of sporadic cases G. BarbujaniA. RussoI. Hausmanova Petrusewicz Original Investigations Pages: 522 - 526
Cell type-dependent difference in the distribution and frequency of excess thymidine-induced common fragile sites: T lymphocytes and skin fibroblasts Akira KuwanoIchiro MuranoTadashi Kajii Original Investigations Pages: 527 - 531
Cytogenetic characterization of ataxia telangiectasia (AT) heterozygotes using lymphoblastoid cell lines and chronic γ-irradiation Manjula WaghraySultan Al-SedairyMohammed A. Hannan Original Investigations Pages: 532 - 534
Kinetochore formation in experimentally undercondensed chromosomes Thomas HaafMichael Schmid Original Investigations Pages: 535 - 538
Phocomelia and additional anomalies in two sisters A. Schinzel Original Investigations Pages: 539 - 541
Localization of the human oncogene SPI1 on chromosome 11, region p11.22 Nguyen Van CongD. RayF. Moreau-Gachelin Original Investigations Pages: 542 - 546
Prophase of meiosis in human spermatocytes analysed by EM microspreading in infertile men and their controls and comparisons with human oocytes R. M. SpeedA. C. Chandley Original Investigations Pages: 547 - 554
Unusual features in the inheritance of ataxia telangiectasia C. G. WoodsS. E. BundeyA. M. R. Taylor Original Investigations Pages: 555 - 562
Variation in the size of human apolipoprotein(a) is due to a hypervariable region in the gene Gisela LindahlElisabeth GersdorfGerd Utermann Original Investigations Pages: 563 - 567
Genetic polymorphisms of gene conversion within the duplicated human α-globin loci Hitoshi NakashimaAsao FujiyamaTakashi Imamura Short Communications Pages: 568 - 570
Screening for steroid sulfatase (STS) gene deletions by multiplex DNA amplification Andrea BallabioJoel E. RanierC. Thomas Caskey Short Communications Pages: 571 - 573
Partial trisomy of the distal segment of 14q Yasuhiro NakamuraKyoko SakaiMasao Yamada Clinical Case Reports Pages: 574 - 576
Female with hypohidrotic ectodermal dysplasia and de novo (X;9) translocation Kay D. MacDermotMaj Hultén Clinical Case Reports Pages: 577 - 579
A new EcoRI polymorphism at the D21S13 locus S. -M. PulstJ. R. KorenbergM. Carbone OriginalPaper Pages: 580 - 580
Partial correction of chromosome instability in Fanconi anemia by desferrioxamine Martin FootHolger Hoehn Letter to the Editors Pages: 581 - 581
Reply to letter by M. Poot and H. Hoehn Berardino PorfirioBruno Dallapiccola Letter to the Editors Pages: 582 - 583
