Clinical Genetics

Cover image for Clinical Genetics

March 1989

Volume 35, Issue 3

Pages 161–232

  1. Original Article

    1. Top of page
    2. Original Article
    3. Case Report
    4. The Vth Nordic Meeting of Medical Genetics
    5. Letters to the Editors
    6. Announcement
    1. Perinatal and first year follow-up of patients with Prader-Willi syndrome: normal size of hands and feet (pages 161–166)

      David Chitayat, Ellen B. Davis, Barbara C. McGillivray, Michael R. Hayden and Judith G. Hall

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02923.x

    2. Tuberous sclerosis and the relation with renal angiomyolipoma. A genetic study on the clinical aspects (pages 167–173)

      J. G. van Baal, P. Fleury and W. H. Brummelkamp

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02924.x

    3. Chorionic villi sampling for early prenatal diagnosis: an option for the Jewish orthodox community (pages 174–180)

      H. Zakut, R. Zamir, O. Yemini, L. Sindel and G. Kohn

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02925.x

    4. Phenotypical features of an unique Irish family with severe autosomal recessive Osteogenesis imperfecta (pages 181–190)

      E. Mair Williams, Alan C. Nicholls, Sara C. M. Daw, Nan Mitchell, L. Stefan Levin, Bryan Green, Janet MacKenzie, Dewi-R. Evans, Patricia A. Chudleigh and F. Michael Pope

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02926.x

    5. Fryns syndrome: report on 8 new cases (pages 191–201)

      S. Aymé, C. Julian, D. Gambarelli, B. Mariotti, A. Luciani, N. Sudan, N. Maurin, N. Philip, F. Serville, D. Carles, M. Rolland and F. Giraud

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02927.x

  2. Case Report

    1. Top of page
    2. Original Article
    3. Case Report
    4. The Vth Nordic Meeting of Medical Genetics
    5. Letters to the Editors
    6. Announcement
    1. Autosomal dominant inheritance in familial angiolipomatosis (pages 202–204)

      Ramesh Kumar, Brian J. G. Pereira, V. Sakhuja and K. S. Chugh

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02928.x

    2. 3C syndrome: third occurrence of cranio-cerebello-cardiac dysplasia (Ritscher-Schinzel syndrome) (pages 205–208)

      A. Verloes, M.-F. Dresse, M. Jovanovic, P. Dodinval and F. Geubelle

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02929.x

  3. The Vth Nordic Meeting of Medical Genetics

    1. Top of page
    2. Original Article
    3. Case Report
    4. The Vth Nordic Meeting of Medical Genetics
    5. Letters to the Editors
    6. Announcement
  4. Letters to the Editors

    1. Top of page
    2. Original Article
    3. Case Report
    4. The Vth Nordic Meeting of Medical Genetics
    5. Letters to the Editors
    6. Announcement
    1. Prader-Willi syndrome and Sotos syndrome (pages 228–229)

      I. Kennerknecht

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02931.x

  5. Announcement

    1. Top of page
    2. Original Article
    3. Case Report
    4. The Vth Nordic Meeting of Medical Genetics
    5. Letters to the Editors
    6. Announcement
    1. Genetics Short Course (page 232)

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02935.x

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