Clinical Genetics

Cover image for Clinical Genetics

February 1990

Volume 37, Issue 2

Pages 81–160

  1. Original Article

    1. Top of page
    2. Original Article
    3. Case Report
    4. Letters to the Editors
    1. Fraser syndrome (cryptophthalmos with syndactyly) in the fetus and newborn (pages 84–96)

      Mette Ramsing, Helga Rehder, Wolfgang Holzgreve, Peter Meinecke and Widukind Lenz

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03484.x

    2. The phakomatoses as paracrine growth disorders (paracrinopathies) (pages 97–105)

      Boris G. Kousseff

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03485.x

    3. Use of the RB1 cDNA as a diagnostic probe in retinoblastoma families (pages 117–126)

      Audrey D. Goddard, Robert A. Phillips, Valerie Greger, Eberhard Passarge, Wolfgang Höpping, Xiaoping Zhu, Brenda L. Gallie and Bernhard Horsthemke

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03488.x

    4. Deletion of chromosome 1p: a short review (pages 127–131)

      P. J. Howard and M. Porteus

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03489.x

    5. Prenatal diagnosis in Pelizaeus-Merzbacher disease using RFLP analysis (pages 141–146)

      Johanna Mäenpää, Elina Lindahl, Pertti Aula and Marja-Liisa Savontaus

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03491.x

  2. Case Report

    1. Top of page
    2. Original Article
    3. Case Report
    4. Letters to the Editors
    1. Trisomy 17p due to a t(8; 17) (p23; p11.2)pat translocation. Case report and review of the literature (pages 148–152)

      C. Schrander-Stumpel, J. Schrander, J. P. Fryns and G. Hamers

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03492.x

    2. 5p;12q translocation with manifestations of cri du chat syndrome and Marfanoid arachnodactyly (pages 153–157)

      Sjzhong Zhang, Yongcai Tang, Fupjng Dai and Erik Nœbuhr

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03493.x

  3. Letters to the Editors

    1. Top of page
    2. Original Article
    3. Case Report
    4. Letters to the Editors
    1. Complex familial translocation (pages 158–159)

      Ricardo Cruz-Coke

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03494.x

    2. On the familial occurrence of congenital bilateral absence of vas deferens (page 159)

      Simone Gilgenkrantz, P. Guillemin and B. Kimmel

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03495.x

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