Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment Michael KrawczakDavid N. Cooper Original investigations Pages: 425 - 441
A t(Y;15) translocation with a deletion of the proximal Yq in a boy with mixed gonadal dysgenesis Mitsuru ShinoharaShigeru MinowadaYasuo Nakagome Original investigations Pages: 442 - 444
Family studies of the LDL receptor gene of relatively severe hereditary hypercholesterolemia associated with Achilles tendon xanthomas Kimiko YamakawaHisako YanagiHideo Hamaguchi Original investigations Pages: 445 - 449
Polymorphism of the T-cell receptor gamma variable and constant region genes in a Chinese population N. GhanemZ. SouaM.-P. Lefranc Original investigations Pages: 450 - 456
Assessment of a creatine kinase isoform M defect as a cause of myotonic dystrophy and the characterization of two novel CKMM polymorphisms Jane BaillyAlex E. MacKenzieRobert G. Korneluk Original investigations Pages: 457 - 462
Genotype-phenotype relationship in various degrees of arylsulfatase A deficiency Joachim KapplerPeter LeinekugelPeter Propping Original investigations Pages: 463 - 470
Changes of common fragile sites on chromosomes according to the menstrual cycle Takashi FuruyaJun HagiwaraShaw Watanabe Original investigations Pages: 471 - 474
High recurrence of rearrangements involving chromosome 14 in an ataxia telangiectasia lymphoblastoid cell line and in its mutagen-treated derivatives Danielle LefrançoisNadja KokaljBernard Dutrillaux Original investigations Pages: 475 - 480
Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the “critical segment” towards the telomere Maria AnvretMagnus NordenskjöldKaren Bröndum-Nielsen Original investigations Pages: 481 - 483
Chromosomal in situ suppression hybridization after Giemsa banding Martin KleverCaspar Grond-GinsbachTraute M. Schroeder-Kurth Original investigations Pages: 484 - 486
Non-radioactive in situ hybridization pattern of the M13 minisatellite sequences on human metaphase chromosomes A. ChristmannP. J. L. LagodaK. D. Zang Original investigations Pages: 487 - 490
Karyotype pecularities of human colorectal adenocarcinomas L. N. KonstantinovaE. W. FleischmanB. P. Kopnin Original investigations Pages: 491 - 496
Molecular analysis of chromosome region 11p13 in patients with Drash syndrome L. JadresicR. B. WadeyJ. K. Cowell Original investigations Pages: 497 - 501
Autosomal dominant retinitis pigmentosa: a new multi-allelic marker (D3S621) genetically linked to the disease locus (RP4) Rajendra Kumar-SinghDaniel G. BradleyPeter Humphries Original investigations Pages: 502 - 504
Frequent deletions at Xq28 indicate genetic heterogeneity in Hunter syndrome Peter J. WilsonGraeme K. SuthersJohn J. Hopwood Original investigations Pages: 505 - 508
The human aldose reductase gene maps to chromosome region 7q35 Alexander GrahamPaul HeathAlexander F. Markham Original investigations Pages: 509 - 514
The human placental protein 14 (PP14) gene is localized on chromosome 9q34 Nguyen Van CongChristian VaisseAlain Bernheim Original investigations Pages: 515 - 518
Duplications of the X chromosome in males: evidence that most parts of the X chromosome can be active in two copies Malgorzata SchmidtDesirée Du SartDaniela Toniolo Original investigations Pages: 519 - 521
DNA polymorphisms associated with a new α1-antitrypsin PI Q0 variant (PI Q0riedenburg) W. PollerJ.-P. FaberK. Olek Short communication Pages: 522 - 524
Localization of DNA probes tightly linked to the Friedreich's ataxia locus by in situ hybridization in a case of pericentric inversion of chromosome 9 Elena RaimondiPia BernasconiMassimo Pandolfo Short communication Pages: 525 - 528
The gene for MEN 2A is tightly linked to the centromere of chromosome 10 Steven A. NarodHagay SobolGilbert M. Lenoir Short communication Pages: 529 - 531
Hunter syndrome in Jews in Israel: further evidence for prenatal selection favoring the Hunter allele J. ZlotogoraT. SchaapG. Bach Short communication Pages: 531 - 533
A de novo unbalanced reciprocal translocation identified as paternal in origin in the Prader-Willi syndrome A. SmithR. LindemanR. J. Trent Clinical case report Pages: 534 - 536
Localisation of RFLPs of the medium chain acyl-CoA dehydrogenase gene Alexandra I. F. BlakemoreSteen KolvraaDiana Curtis OriginalPaper Pages: 537 - 538
High incidence of acute infantile spinal atrophy in Hungary Andrew Czeizel Letter to the editors Pages: 539 - 539
