Clinical Genetics

Cover image for Clinical Genetics

February 1989

Volume 35, Issue 2

Pages 81–160

  1. Original Article

    1. Top of page
    2. Original Article
    3. Case Report
    1. Genetic heterogeneity between two clinical forms of cystic fibrosis evidenced by familial analysis and linked DNA probes (pages 81–87)

      E. Mornet, B. Simon-Bouy, J. L. Serre, F. Muller, A. Taillandier, M. Martinez, J. Boue and A. Boue

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02911.x

    2. Birth prevalence rates of skeletal dysplasias (pages 88–92)

      Claude Stoll, Beatrice Dott, Marie-Paule Roth and Yves Alembik

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02912.x

    3. Bloom's syndrome. XIV. The disorder in Japan (pages 93–110)

      James German and Hiraku Takebe

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02913.x

    4. X chromosome instability associated with familial Turner syndrome (pages 111–115)

      M. Tyrkus, W. H. Hoffman and K. M. Kraemer-Flynn

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02914.x

    5. X-linked spastic paraplegia: evidence for homogeneity with a variable phenotype (pages 116–120)

      Jack Goldblatt, Robea Ballo, Brenda Sachs and Allie Moosa

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02915.x

    6. Ehlers-Danlos syndrome: a new oculo-scoliotic type with associated polyneuropathy? (pages 121–124)

      Talaat I. Farag and R. Neil Schimke

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02916.x

    7. Genetic linkage between Huntington's disease and D4S10(G8) in Scottish families (pages 133–138)

      Susan Holloway, F. A. Millan, Ann Curtis, Moira Mennie and D. J. H. Brock

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02918.x

    8. Chromosomal abnormalities in amniotic fluid cell cultures: a comparison of apparent pseudomosaicism in Chang and RPMI-1640 media (pages 139–145)

      Michael S. Krawczun, Edmund C. Jenkins, Annette Masia, Suphat Kunaporn, Sandra L. Stark, Charlotte J. Duncan, Susan L. Sklower and Raoul D. Rudelli

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02919.x

    9. Autosomal dominant lamellar ichthyosis exhibits an abnormal scale lipid pattern (pages 152–156)

      B. Melnik, W. Küster, J. Hollmann, G. Plewig and H. Traupe

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02921.x

  2. Case Report

    1. Top of page
    2. Original Article
    3. Case Report
    1. Phenotype variability in the Miller acrofacial dysostosis syndrome. Report of two further patients (pages 157–160)

      K. H. Chrzanowska, J. P. Fryns, M. Krajewska-Walasek, L. Wisniewski and H. Van den Berghe

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02922.x

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