Clinical Genetics

Cover image for Clinical Genetics

February 1981

Volume 19, Issue 2

Pages 81–143

  1. Original Article

    1. Top of page
    2. Original Article
    3. Letter to the Editors
    4. Announcements
    1. 49, XYYYY. A case report (pages 87–93)

      L. Sirota, Y. Zlotogora, F. Shabtai, I. Halbrecht and E. Elian

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb00676.x

    2. Clinical and neurophysiological findings in heterozygotes for nonketotic hyperglycinemia (pages 94–100)

      Lennartv. Wendt, Hannu Alanko, Martti Sorri, Erkki Toivakka, Anna-Liisa Saukkonen and Seppo Similä

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb00677.x

    3. Familial X-linked mental retardation and fragile X chromosomes in two Swedish families (pages 101–110)

      K.-H. Gustavson, G. Holmgren, H. K:son Blomquist, M. Mikkelsens, I. Nordenson, H. Poulsen and N. Tommerup

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb00678.x

    4. Athelia in a female infant heterozygous for anhidrotic ectodermal dysplasia (pages 117–121)

      Uta Burck and Karsten R. Held

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb00680.x

    5. Partial trisomy 6q, due to balanced maternal translocation (6;22) (q21; p13) or (q21; pter) (pages 122–125)

      J. Stamberg, J. Shapiro, D. Valle, F. P. Kuhajda, G. Thomas and L. Wissow

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb00681.x

    6. A biastellited marker chromosome in an infant with the caudal regression anomalad (pages 126–129)

      Peter K. A. Jensen and P. Hansen

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb00682.x

    7. Monosomy 10qter due to a balanced familial translocation: t(10;16)(q25.2;q24) (pages 130–133)

      Rolf-Dieter Wegner, Jürgen Kunze and Helmut Paust

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb00683.x

    8. α1-Antitrypsin in patients with hepatocellular carcinoma and chronic active hepatitis (pages 134–139)

      S. Fargion, E. C. Klasen, F. Lalatta, G. Sangalli, M. Tommasini and G. Fiorelli

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb00684.x

  2. Letter to the Editors

    1. Top of page
    2. Original Article
    3. Letter to the Editors
    4. Announcements
    1. No “fragile X” chromosome in normal men (pages 140–141)

      D. Soudek and Nicola Gorzny

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb00685.x

  3. Announcements

    1. Top of page
    2. Original Article
    3. Letter to the Editors
    4. Announcements
    1. Announcements (pages 142–143)

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb00686.x

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