Clinical Genetics

Cover image for Clinical Genetics

February 1988

Volume 33, Issue 2

Pages 65–144

  1. Original Article

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    4. Announcements
    1. A de novo interstitial deletion of chromosome 6 (q22.2q23.1) (pages 65–68)

      Jonathan P. Park, John M. Graham Jr., Susan Z. Berg and Doris H. Wurster-Hill

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb03411.x

    2. EEC syndrome sine sine? : Report of a family with oligosymptomatic EEC syndrome (pages 69–72)

      F. Majewski and W. Küster

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb03412.x

    3. Monosomy, trisomy, fragile sites, and rearrangements of chromosome no. 1 in a mentally retarded male with multiple congenital anomalies (pages 73–77)

      R. L. Neu, B. G. Kousseff, S. Madan, Y.-P. Essig, K. Miller and T. A. Tedesco

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb03413.x

    4. Bardet-Biedl and Laurence-Moon syndromes in a mixed Arab population (pages 78–82)

      Talaat I. Farag and AHW S. TEEBI

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb03414.x

    5. Translocation t(13;14) in nine generations with a case of translocation homozygosity (pages 83–86)

      A. Eklund, K. O. J. Simola and M. Ryynänen

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb03415.x

    6. Male transmission of Apert syndrome (pages 87–90)

      B. R. Rollnick

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb03416.x

    7. A new rare heritable fragile site at 8q24.1 found in a Japanese population (pages 91–94)

      Ei-ichi Takahashi, Tada-aki Hori and Motoi Murata

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb03417.x

    8. A patient with an interstitial deletion of the short arm of chromosome 6 (pages 95–101)

      E. van Swaay, G. C. Beverstock and J. J. P. van de Kamp

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb03418.x

    9. Variability gene effect on cholesterol at the Kidd blood group locus (pages 102–107)

      Kåre Berg

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb03419.x

    10. Partial deletion of the short arm of chromosome 20: 46,XX,del(20)(p11)/46,XX mosaicism (pages 108–110)

      Margherita Cirillo Silengo, Graciela Lopez Bell, M. Biagioli and P. Franceschini

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb03420.x

    11. Microdeletions in patients with X-linked muscular dystrophy: molecular-clinical correlations (pages 131–139)

      M. Lindlöf, H. Kääriäinen, G. J. B. van Ommen and A. de la Chapelle

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb03424.x

  2. Letters to the Editors

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    4. Announcements
    1. Deletion of the short arm of chromosome 20 (pages 140–141)

      P. Kiss and Magda Osztovics

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb03425.x

    2. Oro-facial-digital syndrome II (pages 141–142)

      Yves Gillerot and Lucien Koulischer

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb03426.x

    3. X-linked retinoschisis and linkage (page 143)

      Andreas Gal

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb03427.x

  3. Announcements

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    4. Announcements
    1. Announcements (page 144)

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1988.tb03428.x

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