Clinical Genetics

Cover image for Clinical Genetics

April 1987

Volume 31, Issue 4

Pages 199–278

  1. Original Article

    1. Top of page
    2. Original Article
    3. Short Communication
    4. Letter to the Editors
    5. Announcements
    1. A new interstitial deletion of chromosome No. 4 del(4) (q22::q25) (pages 199–205)

      L. J. Butler, A. V. Palmer, T. Spencer, R. Tabios-Broadway and W. J. Wall

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb02796.x

    2. Contribution to the 18q- syndrome. A patient with del (18) (q22.3qter) (pages 206–210)

      I. Felding, U. Kristoffersson, H. Sjöström and O. Norén

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb02797.x

    3. Diagnosis of arylsulfatase A deficiency in intact cultured cells using a fluorescent derivative of cerebroside sulfate (pages 211–217)

      Gideon Bach, Arie Dagan, Barbara Herz and Shimon Gatt

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb02798.x

    4. Adult Turner syndrome associated with chylous ascites and vascular anomalies (pages 218–223)

      Jonathan Treisman and Francis S. Collins

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb02799.x

    5. Kallmann syndrome associated with choanal atresia (pages 224–227)

      Victor R. Klein, Jan M. Friedman, Gail S. Brookshire, Orval E. Brown and Clare D. Edman

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb02800.x

    6. A phenotypic male with true hermaphroditism and a 46,XX/46,XY/ 47,XXY karyotype (pages 243–248)

      J. M. Wit, A. O. Quartero, N. M. A. Bax and J. Huber

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb02802.x

    7. Molecular heterogeneity of translocations associated with muscular dystrophy (pages 265–272)

      Y. Boyd, E. Munro, P. Ray, R. Worton, T. Monaco, L. Kunkel and I. Craig

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb02805.x

  2. Short Communication

    1. Top of page
    2. Original Article
    3. Short Communication
    4. Letter to the Editors
    5. Announcements
    1. A final word on the tricho-rhino-phalangeal syndromes (pages 273–275)

      E. M. Bühler, U. K. Bühler, C. Beutler and R. Fessler

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb02806.x

  3. Letter to the Editors

    1. Top of page
    2. Original Article
    3. Short Communication
    4. Letter to the Editors
    5. Announcements
    1. Becker's allelic model to explain unusual pedigrees with spinal muscular atrophy (pages 276–277)

      Klaus Zerres, Martina Stephan, Ulrich Kehren and Tiemo Grimm

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb02807.x

  4. Announcements

    1. Top of page
    2. Original Article
    3. Short Communication
    4. Letter to the Editors
    5. Announcements

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