Clinical Genetics

Cover image for Clinical Genetics

January 1990

Volume 37, Issue 1

Pages 1–80

  1. Editorial

    1. Top of page
    2. Editorial
    3. Review
    4. Case Report
    5. Short Communication
    6. Letters to the Editors
    1. Molecular Genetics of Diseases: Clinical Applications (page 1)

      Jan Mohr

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03382.x

  2. Review

    1. Top of page
    2. Editorial
    3. Review
    4. Case Report
    5. Short Communication
    6. Letters to the Editors
    1. Diagnostic molecular genetics of the fragile X (pages 2–11)

      Grant R. Sutherland and John C. Mulley

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03383.x

    2. RFLP analysis for diagnosis of haemophilia A in the German Democratic Republic (pages 12–17)

      F. H. Herrmann, M. Wehnert and K. Wulff

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03384.x

    3. A new syndrome of familial short stature, small hands, valvular heart disease and a characteristic facies (pages 18–23)

      F. A. Collins, M. W. Partington, D. Mulcahy and G. Turner

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03385.x

    4. Consanguinity and the genetic control of Down syndrome (pages 24–29)

      Hanan A. Hamamy, Zuhair S. Al-Hakkak and Salma Al-Taha

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03386.x

    5. Metachromatic leukodystrophy in Greece: observations on 4 cases (pages 30–34)

      Helen Michelakakis, Evagelia Dimitriou, Ch. Bartsocas, Angeliki Skardoutsou and S. Giouroukos

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03387.x

    6. Maternal serum markers in screening for Down syndrome (pages 35–43)

      Bent Nørgaard-Pedersen, Severin Olesen Larsen, Jørgen Arends, Birgit Svenstrup and Ann Tabor

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03388.x

    7. Clinical considerations in Buschke-Ollendorff syndrome (pages 59–63)

      Ian R. Walpole and Prudence J. Manners

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03391.x

  3. Case Report

    1. Top of page
    2. Editorial
    3. Review
    4. Case Report
    5. Short Communication
    6. Letters to the Editors
    1. Skin mastocytosis with short stature, conductive hearing loss and microtia: a new syndrome (pages 64–68)

      B. Wolach, A. Raas-Rothschild, A. Metzker, L. Choc, R. Straussberg, S. Lew and R. M. Goodman

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03392.x

    2. Premature centromeric divisions and prominent telomeres in a patient with persistent Mullerian duct syndrome (pages 69–73)

      G. V. Rangnekar, B. M. Loya, L. K. Goswami and L. K. Sengupta

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03393.x

  4. Short Communication

    1. Top of page
    2. Editorial
    3. Review
    4. Case Report
    5. Short Communication
    6. Letters to the Editors
    1. Lack of specificity of DA/DAPI fluorescence (pages 74–77)

      M. S. Lin, K. H. Huynh, A. Fujimoto and M. G. Wilson

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03394.x

  5. Letters to the Editors

    1. Top of page
    2. Editorial
    3. Review
    4. Case Report
    5. Short Communication
    6. Letters to the Editors
    1. Charcot-Marie-Tooth disease: call for patients (pages 79–80)

      Christine van Broeckhoven

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03396.x

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