Clinical Genetics

Cover image for Clinical Genetics

December 1978

Volume 14, Issue 6

Pages 317–396

  1. Original Article

    1. Top of page
    2. Original Article
    3. Abstract
    1. ABO and Rh phenotyping of foetal blood obtained by foetoscopy (pages 324–329)

      John Philip, Niels Jacob Brandt, Alvito Fernandes, Erik Freiesleben and Dyre Trolle

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1978.tb02097.x

    2. The dermatoglyphic pattern of the trisomy 10p syndrome (pages 330–337)

      A. Rodewald and S. Stengel-Rutkowski

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1978.tb02098.x

    3. Renal dysplasia and asplenia in two sibs (pages 338–344)

      M. d‘A. Crawfurd

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1978.tb02099.x

    4. Cri-du-chat syndrome in a child with a 5/15 translocation and interstitial centromeric heterochromatin (pages 345–350)

      H. J. Gebauer, B. Stumpf, I. Hansmann and T. Grimm

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1978.tb02100.x

    5. Ketotic hypoglycemia in the Penta X and other chromosome imbalance syndromes (pages 367–369)

      Sri Moedjono, William S. Sly, Lawrence B. Mauldin and Morey Haymond

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1978.tb02103.x

    6. Urinary tract malformation in the XYY male (pages 370–372)

      G. A. Machin

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1978.tb02104.x

  2. Abstract

    1. Top of page
    2. Original Article
    3. Abstract

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