Clinical Genetics

Cover image for Clinical Genetics

April 1989

Volume 35, Issue 4

Pages 233–312

  1. Original Article

    1. Top of page
    2. Original Article
    3. Case Report
    4. Abstracts
    5. Letters to the Editors
    1. Two other cases of ANOTHER syndrome? Family report and update (pages 237–242)

      Marta Pinheiro, Francisco José Penna and N. Freire-Maia

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02937.x

    2. Variant nucleolus organizing regions and the risk of Down syndrome (pages 243–250)

      Jeffrey E. Green, Kenneth N. Rosenbaum, Stanley I. Rapoport, Mark B. Schapiro and Beverly J. White

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02938.x

    3. Molecular deletions in the Duchenne/Becker muscular dystrophy gene (pages 251–260)

      Kevin A. Hart, Stephen Abbs, Martin C. Wapenaar, Charlotte G. Cole, Shirley V. Hodgson and Martin Bobrow

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02939.x

    4. Brachydactyly type A-7 (Smorgasbord): a new entity (pages 261–267)

      Samuel A. Meiselman, Michal Berkenstadt, Tami Ben-Ami and Richard M. Goodman

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02940.x

    5. On the familial occurrence of congenital bilateral absence of vas deferens (pages 268–271)

      A. Kleczkowska, J. P. Fryns, O. Steeno and H. van den Berghe

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02941.x

    6. Sjögren-Larsson syndrome in Sweden: distribution of the gene (pages 272–275)

      L. Iselius and S. Jagell

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02942.x

  2. Case Report

    1. Top of page
    2. Original Article
    3. Case Report
    4. Abstracts
    5. Letters to the Editors
    1. An interstitial deletion of the long arm of chromosome 13 (pages 276–281)

      B. Roland, R. B. Lowry, A. S. Robertson and D. M. Cox

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02943.x

    2. Trisomy 5 mosaicism in amniotic fluid with normal outcome (pages 282–284)

      Anthony C. Casamassima, Patrick L. Wilmot, Maurice J. Mahoney, Robin V. Scott and Lawrence R. Shapiro

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02944.x

    3. A 45,X/69,XXY fetus (pages 285–288)

      David R. Betts, Claudine N. Fear, Teresa Barby and Mary J. Seller

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02945.x

    4. A new case of deletion 1q42 syndrome (pages 289–292)

      E. Tolkendorf, G. K. Hinkel and A. Gabriel

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02946.x

    5. Trisomy 9q3 syndrome: a case report and review of the literature (pages 293–298)

      K. Naritomi, Y. Izumikawa, Y. Goya, M. Gushiken, N. Shiroma and K. Hirayama

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02947.x

  3. Abstracts

    1. Top of page
    2. Original Article
    3. Case Report
    4. Abstracts
    5. Letters to the Editors
    1. Prader-Willi Syndrome Scientific Conference III Abstracts (pages 299–309)

      Bryan D. Hall

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02948.x

  4. Letters to the Editors

    1. Top of page
    2. Original Article
    3. Case Report
    4. Abstracts
    5. Letters to the Editors
    1. Dermatoglyphic features of a male with diploid/tetraploid mosaicism (pages 310–311)

      B. Bernhard Wittwer and H. Bärbel Wittwer

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02949.x

    2. Nonsyndromal microphthalmia (pages 311–312)

      Ahmad S. Teebi and Qusay A. Al-Saleh

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1989.tb02950.x

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