Complex translocations, simple variant translocations and Ph-negative cases in chronic myelogenous leukaemia J. L. Huret Review Article Pages: 565 - 568
Identification and characterization of normal length nonfluorescent Y chromosomes: cytogenetic analysis, Southern hybridization and non-isotopic in situ hybridization Frank SpelemanBart Van der AuweraJules Leroy Original Investigations Pages: 569 - 575
Regional assignment of the human thymidylate synthase (TS) gene to chromosome band 18p11.32 by nonisotopic in situ hybridization Tada-aki HoriEi-ichi TakahashiTakeshi Seno Original Investigations Pages: 576 - 580
Direct carrier detection by in situ suppression hybridization with cosmid clones of the Duchenne/Becker muscular dystrophy locus T. RiedV. MahlerM. Cremer Original Investigations Pages: 581 - 586
Localization of the gene for amiloride binding protein on chromosome 7 and RFLP analysis in cystic fibrosis families Pascal BarbryBrigitte Simon-BouyMichel Lazdunski Original Investigations Pages: 587 - 589
X chromosome imprinting in fragile×syndrome Wei-Dong YuSharon L. WengerMark W. Steele Original Investigations Pages: 590 - 594
Molecular nature of chromosome 5q loss in colorectal tumors and desmoids from patients with familial adenomatous polyposis Mieko OkamotoChieko SatoMichiko Miyaki Original Investigations Pages: 595 - 599
Crossovers within a short DNA sequence indicate a long evolutionary history of the APRT*J mutation Naoyuki KamataniShoko KuroshimaYuji Hidaka Original Investigations Pages: 600 - 604
Characteristic chromosome abnormalities, including rearrangements of 6p, del(7q), +12, and t(12;14), in 44 uterine leiomyomas Mef NilbertSverre HeimFelix Mitelman Original Investigations Pages: 605 - 611
Distal trisomy 14q Simone GilgenkrantzJacqueline VigneronMarie-Paule Lefranc Original Investigations Pages: 612 - 616
Distal trisomy 14q Genoveva KeyeuxSimone GilgenkrantzMarie-Paule Lefranc Original Investigations Pages: 617 - 622
Prenatal diagnosis of familial amyloidotic polyneuropathy: evidence for an early expression of the associated transthyretin methionine 30 Maria Rosário AlmeidaIsabel Longo AlvesMaria João M. Saraiva Original Investigations Pages: 623 - 626
Evidence that expression of SpαI/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous α-spectrin allele D. GuetarniA.-F. RouxJ. Godet Original Investigations Pages: 627 - 630
Acute intermittent porphyria caused by a C→T mutation that produces a stop codon in the porphobilinogen deaminase gene G. A. ScobieD. H. LlewellynG. H. Elder Original Investigations Pages: 631 - 634
Clinical and genetic heterogeneity in retinitis pigmentosa Josseline KaplanDominique BonneauJean-Louis Dufier Original Investigations Pages: 635 - 642
A multigene deletion in the immunoglobulin heavy chain region in a highly atopic individual Michael A. WalterCynthia A. ChambersDiane W. Cox Original Investigations Pages: 643 - 647
Analysis of non-disjunction in sex chromosome tetrasomy and pentasomy Terry HassoldDorothy PettayArthur Robinson Original Investigations Pages: 648 - 650
The human aminopeptidase N gene: isolation, chromosome localization, and DNA polymorphism analysis Valerie M. WattHuntington F. Willard Original Investigations Pages: 651 - 654
Detection of a novel point mutation causing haemophilia A by PCR/direct sequencing of ectopically-transcribed factor VIII mRNA Lutz-Peter BergKerstin WielandDavid N. Cooper Original Investigations Pages: 655 - 658
Fragile×expression and×inactivation Doris WöhrleJean-Pierre FrynsPeter Steinbach Original Investigations Pages: 659 - 665
A ZFY-negative 46,XX true hermaphrodite is positive for the Y pseudoautosomal boundary Ralf J. JägerCecilia EbenspergerGerd Scherer Short Communications Pages: 666 - 668
Localisation of a cDNA clone for human cytokeratin 18 to chromosome 17p11–p12 by in situ hybridisation P. HeathP. ElvinA. Markham Short Communications Pages: 669 - 670
A new HaeIII polymorphism at the D21S13 locus S. -M. PulstJ. R. KorenbergJ. Greenwald OriginalPaper Pages: 671 - 671
Cytogenetic studies of chromosome aberrations Patricia A. Jacobs Letters to the Editors Pages: 672 - 674
Chromosomal damage in lymphocytes and fibroblasts of patients treated for testicular cancer C. D. DeLozier-Blanchet Letters to the Editors Pages: 675 - 676
An informative polymorphism detectable by polymerase chain reaction at the 3′ end of the dystrophin gene C. OudetR. HeiligJ. L. Mandel Erratum Pages: 677 - 677