Clinical Genetics

Cover image for Clinical Genetics

October 1986

Volume 30, Issue 4

Pages 241–352

  1. Original Article

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    4. Announcements
    1. High-resolution cytogenetic studies in patients with Prader-Willi syndrome (pages 241–248)

      Takako Takano, Yasuo Nakagome, Shigeo Nagafuchi, Fumihiko Tanaka, Yasuhide Nakamura, Tetsu Nagano, Ayako Tanae and Itsuro Hibi

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00603.x

    2. Analysis of fragile X-mental retardation families using flanking polymorphic DNA probes (pages 249–254)

      P. Goonewardena, K.-H. Gustavson, G. Holmgren, A. Tolun, J. Chotai, E. Johnsen and U. Pettersson

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00604.x

    3. Distal 11q monosomy. The typical 11q monosomy syndrome is due to deletion of subband 11q24.1 (pages 255–260)

      J. P. Fryns, A. Kleczkowska, M. Buttiens, P. Marien and H. VAN DEN Berghe

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00605.x

    4. Inbreeding and schizophrenia (pages 261–275)

      L. Saugstad and Ø. ØDegård

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00606.x

    5. Recombination aneusomy of chromosome 5 associated with multiple severe congenital malformations (pages 285–292)

      H. W. Schroeder JR., S. Forbes, L. Mack, S. Davis and T. H. Norwood

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00608.x

    6. The arylsulphatases of chorionic villi: potential problems in the first-trimester diagnosis of metachromatic leucodystrophy and Maroteaux-Lamy disease (pages 302–308)

      N. Sanguinetti, Jane Marsh, Marie Jackson, A. H. Fensom, R. C. Warren and C. H. Rodeck

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00611.x

    7. St. Helena familial genu valgum (pages 309–314)

      P. Beighton, H. S. Myers, S. J. Aldridge, J. Sedgewick and S. Eickhoff

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00612.x

    8. A genetic-diagnostic survey in an institutionalized population of 173 severely mentally retarded patients (pages 315–323)

      J. P. Fryns, A. Kleczkowska, A. Dereymaeker, M. Hoefnagels, G. Heremans, J. Marien and H. VAN DEN Berghe

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00613.x

    9. Effect of sibship position on reproductive behavior of couples after the birth of a genetically handicapped child (pages 328–334)

      M. W. Steele, L. Rosser, J. B. Rodnan and M. Bryce

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00615.x

    10. Oto-Palato-Digital syndrome in four generations of a larqe family (pages 338–344)

      Uco E. Pazzaglia and Giampiero Beluffi

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00617.x

  2. Letters to the Editors

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    4. Announcements
    1. In defence of partial trisomy (pages 345–346)

      R.J.M. Gardner

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00619.x

    2. Congenital cutis laxa (page 345)

      John Rogers and David Danks

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00618.x

    3. Fragile X; experience of a laboratory (pages 346–347)

      D. Soudek

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00620.x

    4. Mutation of the Duchenne muscular dystrophy gene associated with meiotic recombination (pages 347–349)

      E. Bakker and Prof. dr. P. L. Pearson

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00621.x

  3. Announcements

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    4. Announcements
    1. Announcements (pages 350–352)

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00622.x

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