Clinical Genetics

Cover image for Clinical Genetics

October 1988

Volume 34, Issue 4

Pages 209–282

  1. Original Article

    1. Top of page
    2. Original Article
    3. Letter to the Editors
    4. Announcements
    1. PRUFILE: a clinical and laboratory database for the genetics centre (pages 209–218)

      D. E. Mutton, K. Chown, L. Thomson, A. C. Berry, P. K. Botcherby and M. Bobrow

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb02867.x

    2. Terminal deletion of the short arm of chromosome 5 (pages 219–223)

      C. Baccichetti, E. Lenzini, L. Artifoni, D. Caufin and P. Marangoni

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb02868.x

    3. Trisomy (1q) (q42[RIGHTWARDS ARROW]qter): confirmation of a syndrome (pages 224–229)

      N. L. Chia, L. R. Bousfield, C. C. S. Poon and B. J. Trudinger

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb02869.x

    4. Coffin-Lowry syndrome: a multicenter study (pages 230–245)

      S. Gilgenkrantz, P. Mujica, P. Gruet, P. Tridon, F. Schweitzer, A. Nivelon-Chevallier, J. L. Nivelon, G. Couillault, A. David, A. Verloes, C. Lambotte, Ch. Piussan and M. Mathieu

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb02870.x

    5. Apolipoprotein E alleles and hyperlipoproteinemia in Japan (pages 246–251)

      M. Eto, K. Watanabe and K. Ishii

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb02871.x

    6. Association of apolipoprotein ɛ4 allele with hypertriglyceridemia in obesity (pages 258–264)

      F. Fumeron, D. Rigaud, M. C. Bertiere, S. Bardon, C. Dely and M. Apfelbaum

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb02873.x

    7. Infantile autism, fragile (X) (q27.3) and RFLP analysis in an extended Swedish family (pages 265–271)

      Maria Anvret, Christopher Gillberg, Jan Wahlström, Kerstin Albertsson-Wikland and Kay Davies

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb02874.x

    8. Marner's cataract (CAM) assigned to chromosome 16: linkage to haptoglobin (pages 272–275)

      Hans Eiberg, Else Marner, Thomas Rosenberg and Jan Mohr

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb02875.x

  2. Letter to the Editors

    1. Top of page
    2. Original Article
    3. Letter to the Editors
    4. Announcements
    1. A photometer used for diagnosing a small-sized 4p deletion in Wolf syndrome (pages 276–278)

      C. Léonard and J. L. Huret

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb02876.x

    2. Mental retardation with pterygia, shortness and distinct facial appearance. Confirmation of a new MCA/MR syndrome (pages 279–281)

      C. Schrander-Stumpel, M. Haspeslagh and J. P. Fryns

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb02877.x

  3. Announcements

    1. Top of page
    2. Original Article
    3. Letter to the Editors
    4. Announcements
    1. Announcements (page 282)

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb02878.x

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