Clinical Genetics

Cover image for Clinical Genetics

February 1980

Volume 17, Issue 2

Pages 97–176

  1. Original Article

    1. Top of page
    2. Original Article
    3. Announcement
    1. Dominant sex-linked inherited chondrodysplasia punctata: a distinct type of chondrodysplasia punctata (pages 97–107)

      H. Manzke, E. Christophers and H.-R. Wiedemann

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00115.x

    2. Spontaneous and X-ray induced chromosomal aberrations in selected connective tissue diseases (pages 108–114)

      Wesley C. Burkhardt Jr., John F. Jackson, Suthin Songcharoen and Edward F. Meydrech

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00116.x

    3. Penetrance estimates and recurrence risks for fibromuscular dysplasia (pages 115–116)

      K. Gladstien, A. R. Rushton and K. K. Kidd

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00117.x

    4. Upper limb anomalies and renal disease (pages 117–119)

      Richard L. Siegler, Paul Larsen and Bruce A. Buehler

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00118.x

    5. Dermatoglyphic patterns in the Sjögren-Larsson syndrome (pages 120–124)

      K. H. Gustavson and S. Jagell

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00119.x

    6. Familial X-linked mental retardation with a marker X chromosome and its relationship to macro-orchidism (pages 125–128)

      Patricia N. Howard-Peebles and Gayle R. Stoddard

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00120.x

    7. The spectrum of frontonasal dysplasia in an inbred pedigree (pages 137–142)

      H. Moreno Fuenmayor

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00122.x

    8. Bloom's syndrome in a Japanese girl (pages 143–148)

      Hiroko Kawashima, Tamotu Sato, Noboru Taniguchi, Takashi Yagl, Kanzi Ishizaki and Hiraku Takere

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00123.x

    9. Gc Serum groups and schizophrenia (pages 149–152)

      L. Beckman, G. Beckman and C. Perris

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00124.x

    10. Association of severe rheumatoid arthritis with heterozygosity for α-antitrypsin deficiency (pages 153–160)

      Diane Wilson Cox and Olga Huber

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00125.x

    11. Baller-Gerold syndrome Craniosynostosis-radial aplasia syndrome (pages 161–166)

      K. Anyane-Yeboa, L. Gunning and A. D. Bloom

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00126.x

    12. Absent ulna in the Klippel-Feil syndrome: an unusual associated malformation (pages 167–170)

      J. Chemke, R. Nisani and R. E. Fischel

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00127.x

  2. Announcement

    1. Top of page
    2. Original Article
    3. Announcement
    1. Announcement (page 176)

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00129.x

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