Clinical Genetics

Cover image for Clinical Genetics

July 1989

Volume 36, Issue 1

Pages 1–78

  1. Original Article

    1. Top of page
    2. Original Article
    3. Case Report
    4. Letter to the Editor
    1. A familial chromosomal translocation t(6q;7q) with habitual abortions (pages 1–4)

      Sizhong Zhang, Xiaoyan Wu, Qun Ho and Li Zhao

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb03359.x

    2. X-linked myotubular myopathy: clinical and pathological findings in a family (pages 5–14)

      A. Oldfors, M. Kyllerman, J. Wahlström, C. Darnfors and K. G. Henriksson

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb03360.x

    3. A survey of manifesting carriers of Duchenne and Becker muscular dystrophy in Wales (pages 31–37)

      Andrew Norman and Peter Harper

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb03363.x

    4. Leukocyte and plasma N-laurylsphingosine deacylase (ceramidase) in Farber disease (pages 38–42)

      Y. Ben-Yoseph, R. Gagné, M. R. Parvathy, D. A. Mitchell and T. Momoi

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb03364.x

    5. Albinism and skin cancer in Southern Africa (pages 43–52)

      Jennifer G. R. Kromberg, David Castle, Esther M. Zwane and Trefor Jenkins

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb03365.x

    6. An aetiological study of isochromosome-X Turner's syndrome (pages 53–58)

      Andrew D. Carothers, Rhona De Mey, Michael Daker, Elizabeth Boyd, Michael Connor, Patricia M. Ellis and David Stevenson

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb03366.x

  2. Case Report

    1. Top of page
    2. Original Article
    3. Case Report
    4. Letter to the Editor
    1. Angiokeratoma corporis diffusum in GM1 gangliosidosis, Type 1 (pages 59–64)

      Nicholas G. Beratis, Anastasia Varvarigou-Frimas, Stavroula Beratis and Susan L. Sklower

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb03367.x

    2. De novo Robertsonian D/D type translocations: the Leuven experience (pages 65–68)

      A. Kleczkowska, J. P. Fryns, L. Standaert and H. van den Berghe

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb03368.x

    3. Holt-Oram syndrome associated with the hypoplastic left heart syndrome (pages 69–72)

      Tracy A. Glauser, Elaine Zackai, Paul Weinberg and Robert Clancy

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb03369.x

  3. Letter to the Editor

    1. Top of page
    2. Original Article
    3. Case Report
    4. Letter to the Editor
    1. Aarskog syndrome in Hungary (pages 73–74)

      P. Kiss

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb03370.x

    2. Trisomy 1q (pages 75–76)

      P. Kiss and Júlia Imrei

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb03371.x

    3. Another case of Bloom's syndrome in Japan (pages 77–78)

      Satoshi Ishikiriyama

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb03372.x

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