Clinical Genetics

Cover image for Clinical Genetics

August 1984

Volume 26, Issue 2

Pages 81–167

  1. Original Article

    1. Top of page
    2. Original Article
    3. Short Communication
    4. Letter to the Editor
    1. Manifestations and natural history of idiopathic hemihypertrophy: a review of eleven cases (pages 81–86)

      D. Viljoen, J. Pearn and P. Beighton

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00797.x

    2. Selection against genetic defects in semen donors (pages 87–108)

      P. E. Smith

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00798.x

    3. Reduced plasma concentrations of total, low density lipoprotein and high density lipoprotein cholesterol in patients with Gaucher type I disease (pages 109–116)

      Henry Ginsberg, Gregory A. Grabowski, Joyce Corey Gibson, Richard Fagerstrom, Jack Goldblatt, Harriet S. Gilbert and Robert J. Desnick

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00799.x

    4. Fragile 22q13 segregating in a family (pages 125–128)

      T. Webb and A. Thake

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00801.x

    5. Genetics of site specific colon cancer: a family study (pages 129–132)

      R. Bamezai, Gurpreet Singh, N. N. Khanna and Shamer Singh

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00802.x

    6. Combined sialidase (neuraminidase) and β-galactosidase deficiency. Clinical, morphological and enzymological observations in a patient (pages 139–149)

      M. C. B. Loonen, A. J. J. Reuser, P. Visser and W. F. M. Arts

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00804.x

    7. Mosaic tetrasomy 21 in a male child (pages 150–155)

      M. L. Kwee, P. G. Barth, F. Arwert and K. Madan

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00805.x

    8. A young girl with ring(18) mosaicism: cytogenetic studies and PEP A mapping (pages 156–160)

      Mariano Rocchi, Ileana Cigui, Nicoletta Archidiacono, Vanna Pecile, Giovanni Porcelli and Giorgio Filippi

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00806.x

  2. Short Communication

    1. Top of page
    2. Original Article
    3. Short Communication
    4. Letter to the Editor
    1. Prader-Willi syndrome in Black females (pages 161–163)

      Wendy L. Golden, Jeanne M. Hanchett, Nancy Breslin and Mark W. Steele

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00807.x

  3. Letter to the Editor

    1. Top of page
    2. Original Article
    3. Short Communication
    4. Letter to the Editor
    1. Male to male transmission of the G syndrome (page 164)

      J. Chemke, E. Shor, H. Ankori-Cohen and E. Kazuni

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00808.x

    2. Monosomy X associated with fra(17p12) and 22p- (pages 165–166)

      Viliam Izakovič

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00809.x

    3. Chromosome studies on normal males in 16 families with the marker X chromosome (pages 166–167)

      P. A. Venter, D. J. Coetzee, J. Wilmot, D. Behari, S. A. Battson, N. Kritzinger, J. L. Du Toit and J. Op't Hof

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00810.x

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