Clinical Genetics

Cover image for Clinical Genetics

February 1984

Volume 25, Issue 2

Pages 125–220

  1. Original Article

    1. Top of page
    2. Original Article
    3. Abstracts
    4. Letter to the Editor
    1. The psychological profile of the fragile X syndrome (pages 131–134)

      J. P. Fryns, J. Jacobs, A. Kleczkowska and H. van den Berghe

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00474.x

    2. In vitro reversal of fragile-X expression by exogenous thymidine (pages 135–139)

      Gale B. Gardiner, Sharon L. Wenger and Mark W. Steele

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00475.x

    3. Marker chromosomes in parents to children with Down's syndrome (pages 140–147)

      G. Annerén, J. Wahlström and N. Tommerup

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00476.x

    4. Familial minor neurodevelopmental disorders (pages 148–154)

      F. Rasmussen, K.-H. Gustavson and B. Bille

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00477.x

    5. Diagnostic considerations in arthrogry-posis syndromes in South Africa (pages 155–162)

      G. S. Gericke, J. G. Hall, M. M. Nelson and P. H. Beighton

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00478.x

    6. Autosomal recessive inheritance of Charcot-Marie-Tooth disease associated with sensorineural deafness (pages 163–165)

      J. Cornell, S. Sellars and P. Beighton

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00479.x

    7. Bloom's syndrome XI. Progress report for 1983 (pages 166–174)

      James German, David Bloom and Eberhard Passarge

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00480.x

    8. The syndromic status of sclerosteosis and van Buchem disease (pages 175–181)

      P. Beighton, A. Barnard, H. Hamersma and A. van der Wouden

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00481.x

    9. Absent tibiae, triphalangeal thumbs and polydactyly: description of a family and prenatal diagnosis (pages 182–186)

      S. Canún, R. M. Lomelí, R. Martínez and A. Carnevale

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00482.x

    10. A new psychomotor retardation syndrome with peculiar facies and marfan-oid habitus (pages 187–190)

      R. Fragoso and J. M. Cantú

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00483.x

    11. Mucopolysaccharidosis III B: hybridization studies on fibroblasts from a mild case and fibroblasts from severe patients (pages 191–195)

      Andrea Ballabio, Rita Pallini and Paola Di Natale

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00484.x

    12. Ring chromosome 10 syndrome: case report and the possibility of clinical diagnosis (pages 196–200)

      Ikuko Kondo, Yae Shimakura, Takeki Hirano, Michio Kaneko and Keijiro Yabuta

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00485.x

    13. The NEU-COFS (cerebro-oculo-facio-skeletal) syndrome: report of a case (pages 201–204)

      M. C. Silengo, G. Davi, R. Bianco, M. Biagioli, P. Franceschini, M. Cavallo and G. Bussi

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00486.x

  2. Abstracts

    1. Top of page
    2. Original Article
    3. Abstracts
    4. Letter to the Editor
  3. Letter to the Editor

    1. Top of page
    2. Original Article
    3. Abstracts
    4. Letter to the Editor
    1. Letters to the Editors (pages 214–219)

      Lowell R. Weitkamp

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00488.x

    2. Letters to the Editors (pages 219–220)

      L. V. Wendt and S. Similä

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00489.x

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