Clinical Genetics

Cover image for Clinical Genetics

January 1984

Volume 25, Issue 1

Pages 1–123

  1. Original Article

    1. Top of page
    2. Original Article
    3. Letter to the Editor
    4. Announcements
    5. The Human Gene Map
    1. Further delineation of the Cohen syndrome; report on chorioretinal dystrophy, leukopenia and consanguinity (pages 1–14)

      Reuo Norio, Christina Raitta and Elina Lindahl

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00456.x

    2. Ethical and social aspects of risk predictions (pages 25–32)

      John C. Fletcher

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00458.x

    3. Chromosomal constitution of infertile men (pages 33–36)

      Miroslava Mićić, Sava Mićić and Vukosava Diklić

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00459.x

    4. Lchthyosis vulgaris with hypogenitalism and hypogonadism: evidence for different genotypes by lipoprotein electrophoresis and steroid sulfatase testing (pages 42–51)

      H. Traupe, C. R. Müller-Migl, G. Kolde, R. Happle, P. M. Kövary, H. Hameister and H. H. Ropers

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00461.x

    5. Familial balanced insertion (5;10) and monosomy and trisomy (10) (q24.2[RIGHTWARDS ARROW]q25.3) (pages 52–58)

      M. J. van de Vooren, H. T. Planteydt, A. Hagemeijer, M. F. Peters-Slough and M. J. Timmerman

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00462.x

    6. The Schinzel syndrome in a mother and daughter (pages 63–67)

      Jacqueline T. Hecht and Charles I. Scott Jr

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00464.x

    7. Grebe chondrodysplasia and brachydactyly in a family (pages 68–72)

      D. Kumar, D. Curtis and C. E. Blank

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00465.x

    8. A Weaver-like syndrome in a Japanese boy (pages 73–78)

      Masato Tsukahara, Suguru Tanaka and Tadashi Kajii

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00466.x

    9. 46, X, i(Xq)/45, X mosaicism with gonadal dysgenesis associated with 21p- (pages 79–83)

      Magdolna Gaál, A. Tóth, P. Bösze and J. László

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00467.x

  2. Letter to the Editor

    1. Top of page
    2. Original Article
    3. Letter to the Editor
    4. Announcements
    5. The Human Gene Map
    1. Cytogenetics of ring chromosome 7 (pages 84–85)

      Celia D. DeLozier-Blanchet and Rita Guenin

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00468.x

    2. Robertsonian Translocation and Prader-Willi syndrome (page 86)

      Dr. A. Smith

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00469.x

    3. Mohr syndrome variant or Joubert-Boltshauser syndrome? (pages 86–87)

      J. Egger and M. Baraitser

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00470.x

  3. Announcements

    1. Top of page
    2. Original Article
    3. Letter to the Editor
    4. Announcements
    5. The Human Gene Map
  4. The Human Gene Map

    1. Top of page
    2. Original Article
    3. Letter to the Editor
    4. Announcements
    5. The Human Gene Map
    1. The Human Gene Map 15 November 1983 (pages 89–123)

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1984.tb00472.x

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