Clinical Genetics

Cover image for Clinical Genetics

April 1986

Volume 29, Issue 4

Pages 269–348

  1. Original Article

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    4. Announcements
    1. Congenital heart disease in supernumerary der(22), t(11;22) syndrome (pages 269–275)

      Angela E. Lin, Juan Bernar, Alvin J. Chin, Robert S. Sparkes, Beverly S. Emanuel and Elaine H. Zackai

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb01254.x

    2. Cardiovascular manifestations in Fabry's disease : A high incidence of mitral valve prolapse in hemizygotes and heterozygotes (pages 276–283)

      Hitoshi Sakuraba, Yukishige Yanagawa, Takashi Igarashi, Yoshiyuki Suzuki, Tadashi Suzuki, Koji Watanabe, Keiko Ieki, Kosuke Shimoda and Tatsuhiro Yamanaka

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb01255.x

    3. Psychosocial adjustment of adult women with Turner syndrome (pages 284–290)

      Elizabeth McCauley, Virginia P. Sybert and Anke A. Ehrhardt

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb01256.x

    4. Measurement of body fat in Turner syndrome (pages 291–297)

      J. A. Delgado, C. M. Trahms and V. P. Sybert

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb01257.x

    5. The spectrum of clinical features in CHARGE syndrome (pages 298–310)

      Sandra L. H. Davenport, Margaret A. Hefner and Joyce A. Mitchell

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb01258.x

    6. Gonadoblastoma and Y-chromosome fluorescence (pages 311–316)

      T. Lukusa, J. P. Fryns and H. van den Berghe

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb01259.x

    7. The Borjeson-Fbrssman-Lehmann syndrome : A family study (pages 317–320)

      A. M. Dereymaeker, J. P. Fryns, M. Hoefnagels, G. Heremans, J. Marien and H. van den Berghe

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb01260.x

    8. Heterogeneity of Morquio disease (pages 325–331)

      M. Beck, J. Glössl, A. Grubisic and J. Spranger

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb01262.x

    9. Trichodermodysplasia with dental alterations: an apparently new genetic ectodermal dysplasia of the trichoodonto-onychial subgroup (pages 332–336)

      Marta Pinheiro, Dértia V. Freire-Maia, E. Miranda, O. G. Silva-Filho and N. Freire- Maia

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb01263.x

    10. Deleted ring chromosome 22 in a mentally retarded boy (pages 337–341)

      K.-H. Gustavson, W. Arancibia, U. Eriksson and L. Svennerholm

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb01264.x

    11. Multiple congenital anomalies in a child born after prenatal diagnosis of trisomy 20mosaicism (pages 342–344)

      Wolfgang Holzgreve, Mahin Golabi and Joel Bradley

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb01265.x

  2. Letters to the Editors

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    4. Announcements
    1. Absent tibiae, triphalangeal thumbs, Polydactyly and non-penetrance (page 347)

      S. Sonia Canún

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb01267.x

  3. Announcements

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    4. Announcements
    1. Announcements (page 348)

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb01268.x

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