Clinical Genetics

Cover image for Clinical Genetics

September 1987

Volume 32, Issue 3

Pages 145–208

  1. Original Article

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    4. Announcement
    1. Familial absence of the trapezius muscle with associated shoulder girdle abnormalities (pages 145–147)

      E. Gross-Kieselstein and R. S. Shalev

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03344.x

    2. Clinical anophthalmos in a family (pages 156–159)

      A. Sensi, C. Incorvaia, A. Sebastiani and E. Calzolari

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03346.x

    3. Monosomy and trisomy of 15q24[RIGHTWARDS ARROW]qter in a family with a translocation t(6;15)(P25;q24) (pages 169–171)

      Ulf Kristoffersson, Sverre Heim, Nils Mandahl, Lennart Sundkvist, Jan Szelest and Inga Hägerstrand

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03348.x

    4. Type III congenital cystic adenomatoid malformation of the lung: another cause of elevated alpha fetoprotein? (pages 172–174)

      P. Petit, M. Bossens, D. Thomas, Ph Moerman, J. P. Fryns and H. van den Berghe

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03349.x

    5. Three-generation transmission of Hirschsprung's disease (pages 175–178)

      A. H. Lipson and J. Harvey

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03350.x

    6. Fragile (X) syndrome: a study of the psychological profile in 23 prepubertal patients (pages 179–186)

      M. Borghgraef, J. P. Fryns, A. Dlelkens, K. Pyck and H. Van Den Berghe

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03351.x

    7. Evidence for a sperm mutation resulting in Duchenne muscular dystrophy (pages 187–191)

      A. L. Børresen, A. Heiberg, P. Møller and K. Berg

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03352.x

    8. X-linked retinoschisis is closely linked to DXS41 and DXS16 but not DXS85 (pages 192–195)

      Tiina Alitalo, Jussi Kärnä, Henjik Forsius and Albert de la Chapelle

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03353.x

    9. Ehlers-Danlos syndrome: yet another type? (pages 196–201)

      Denis Viljoen, Jack Goldblatt, Dave Thompson and Peter Beighton

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03354.x

    10. Postaxial polydactyly in association with neurofibromatosis (pages 202–205)

      Paul Merlob, Yizhak Levy and Avinoam Shuper

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03355.x

  2. Letters to the Editors

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    4. Announcement
    1. Ichthyosis-cheek-eyebrow syndrome (ICE(skin)) (page 206)

      R. M. Goodman, E. Sidransky and A. Feinstein

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03356.x

    2. Holoprosencephaly associated with ring chromosome 21 (page 207)

      J. M. N. Hoovers and M. C. E. Jansweijer

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03357.x

  3. Announcement

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    4. Announcement
    1. Announcement (page 208)

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03358.x

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