Clinical Genetics

Cover image for Clinical Genetics

March 1993

Volume 43, Issue 3

Pages 113–168

  1. Original Article

    1. Top of page
    2. Original Article
    3. Genetics and Society
    4. Letters to the Editor
    5. Announcement
    1. Multipoint linkage analysis in X-linked juvenile retinosclusis (pages 113–116)

      A. A. B. Bergen, M. J. Van Schooneveld, U. Orth, E. M. Bleeker-Wagemakers and A. Gal

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1993.tb04433.x

    2. Familial complex chromosomal rearrangement resulting in duplication/deletion of 6q1c to 6q16 (pages 117–121)

      B. Roland, R. B. Lowry, O. M. Cox, P. Ferreira and C. C. Lin

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1993.tb04434.x

    3. Nager acrofacial dysostosis: minor familial manifestations supporting dominant inheritance (pages 127–131)

      David T. Bonthron, Donald F. Macgregor and David G. D. Barr

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1993.tb04436.x

    4. Del(2q) — cause of the wrinkly skin syndrome? (pages 132–138)

      Friedmar R. Kreuz and Birbei H. Wittwer

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1993.tb04437.x

    5. Different clinical features in monozygotic twins: a case of 7q — syndrome (pages 139–142)

      H. Tsukamoto, K. Inui, M. Taniike, K. Kamiyama, M. Hori, K. Sumi and S. Okada

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1993.tb04438.x

    6. Late-onset familial amyloid polyneuropathy with the TTR Met 30 mutation in France (pages 143–145)

      Gilles Grateau, David Adams, Denis Malapert, Michele Viemont, Marc Deipech and Gerard Said

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1993.tb04439.x

    7. Huntington's disease: predictive testing and the molecular genetics laboratory (pages 150–156)

      L. P. Lazarou, A. L. Meredith, J. M. Myring, A. Tyler, M. Morris, O. M. Ball and P. S. Harper

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1993.tb04441.x

    8. Affected sibs with fragde X syndrome exhibit an age-dependent decrease in the size of the fragile X full mutation (pages 157–159)

      Etienne Mornet, Mikael Jokle, Any Bogyo, Isabel Tejada, Christianne Deluchat, Joelle Boué and André Boué

      Version of Record online: 10 AUG 2012 | DOI: 10.1111/j.1399-0004.1993.tb04462.x

  2. Genetics and Society

    1. Top of page
    2. Original Article
    3. Genetics and Society
    4. Letters to the Editor
    5. Announcement
  3. Letters to the Editor

    1. Top of page
    2. Original Article
    3. Genetics and Society
    4. Letters to the Editor
    5. Announcement
    1. Exclusion map of the gene for neuraminidase from 10(pter [RIGHTWARDS ARROW] p15.1) (pages 166–167)

      Takako Takano, Hitoshi Horigome and Sawako Shibata

      Version of Record online: 10 AUG 2012 | DOI: 10.1111/j.1399-0004.1993.tb04464.x

    2. Eronen syndrome identical with DOOR syndrome? (page 167)

      R. M. Winter

      Version of Record online: 10 AUG 2012 | DOI: 10.1111/j.1399-0004.1993.tb04465.x

  4. Announcement

    1. Top of page
    2. Original Article
    3. Genetics and Society
    4. Letters to the Editor
    5. Announcement
    1. Announcement (page 168)

      Version of Record online: 10 AUG 2012 | DOI: 10.1111/j.1399-0004.1993.tb04466.x

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