Clinical Genetics

Cover image for Clinical Genetics

October 1984

Volume 26, Issue 4

Pages 281–384

  1. Original Article

    1. Top of page
    2. Original Article
    3. Letter to the Editors
    1. The impact of large Y chromosome on pregnancy, foetus and birth (pages 281–288)

      P. Videbech, J. Nielsen, M. Wohlert, G. Eriksen, K. B. Hansen, L. Hvidman and B. Krag-Olsen

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb01060.x

    2. Chorionic villi sampling under direct vision (pages 297–300)

      Björn Gustavii

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb01062.x

    3. Detection of the fragile X chromosome and other fragile sites (pages 301–303)

      Frederick Hecht and Grant R. Sutherland

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb01063.x

    4. Date of conception and prevention of neural tube defects (pages 304–307)

      Louis Dallaire, Serge B. Melancon, Michel Potier, Jean-P. Mathieu and Gilles Ducharme

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb01064.x

    5. The manifestations and natural history of spondylo-epi-metaphyseal dysplasia with joint laxity (pages 308–317)

      P. Beighton, G. Gericke, K. Kozlowski and L. Grobler

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb01065.x

    6. Fetal mortality in oral cleft families (IX): factors relating to the occurrence of sporadic clefts (pages 322–330)

      Krishna R. Dronamraju, Kahlil G. Wakim, David J. Smith and David Bixler

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb01067.x

    7. Controlled comparison of plasma and serum for cystic fibrosis protein (pages 331–338)

      G. B. Wilson, J. Mc intosh, J. Dietrich and T. Manning

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb01068.x

    8. Del 11p/aniridia complex. Report of three patients and review of 37 observations from the literature (pages 356–362)

      Catherine Turleau, Jean de Grouchy, Marie-France Tournade, Marie-France Gagnadoux and Claudine Junien

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb01071.x

    9. Genital anomaly and cardiomyopathy: a new syndrome (pages 371–373)

      Samir S. Najjar, Vazken M. Der Kaloustian and Kassem O. Ardati

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb01073.x

    10. The Coffin-Siris syndrome: Report of a family and further delineation (pages 374–378)

      M. Haspeslagh, J. P. Fryns and H. van den Berghe

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb01074.x

    11. Duplication in chromosome 15q in a boy with the Prader-Willi syndrome; further cytogenetic confusion (pages 379–382)

      H. F. de France, F. A. Beemer and P. F. Ippel

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb01075.x

  2. Letter to the Editors

    1. Top of page
    2. Original Article
    3. Letter to the Editors
    1. Sensorineural deafness and peripheral neuropathy (pages 383–384)

      Richard M. Pauli

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb01076.x

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