Clinical Genetics

Cover image for Clinical Genetics

April 1994

Volume 45, Issue 4

Pages 165–219

  1. Original Article

    1. Top of page
    2. Original Article
    3. Case Report
    4. Letter to the Editor
    5. Announcement
    1. Fine mapping of X-linked clasped thumb and mental retardation (MASA syndrome) in Xq28 (pages 165–168)

      E. Legius, L. Kaepernick, J. V. Higgins and T. W. Glover

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04016.x

    2. Prader-Willi-like phenotype in fragile X syndrome (pages 175–180)

      Constance Schrander-Stumpel, Willem-Jan Gerver, John Engelen, Hans Mulder and Jean-Pierre Fryns

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04018.x

    3. Clinical aspects of the MASA syndrome in a large family, including expressing females (pages 181–185)

      L. Kaepernick, E. Legius, J. Higgins and S. Kapur

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04019.x

    4. Fragile X syndrome with extra microchromosome (pages 186–189)

      I. López-Pajares, A. Delicado, I. Pascual-Castroviejo, V. López-Martin, F. Moreno and J. A. Garcia-Marcos

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04020.x

    5. Hereditary pubertal genu valgum in Iran (pages 190–193)

      K. Ghorbani and J. Carapetian

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04021.x

    6. The primary hereditary form of distal renal tubular acidosis: clinical and genetic studies in 60-member kindred (pages 194–199)

      Hassen Chaabani, Amel Hadj-Khlil, Naceur Ben-Dhia and Hammadi Braham

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04022.x

    7. Onychotrichodysplasia and chronic neutropenia without mental retardation (ONS): a second case report (pages 200–202)

      B. Dallapiccola, R. Mingarelli and G. Obregon

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04023.x

    8. Partial trisomy and monosomy 8p due to inversion duplication (pages 203–207)

      J. J. M. Engelen, C. E. M. de Die-Smulders, J. P. Fryns, J. M. N. Hoovers, J. C. M. Albrechts, W. J. G. Loots, M. E. Jacobs and A. J. H. Hamers

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04024.x

    9. Effects of consanguinity on anthropometric measurements of newborn infants (pages 208–211)

      N. Başaran, S. Artan, S. Yaziciogllu and B. S. Şayli

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04025.x

  2. Case Report

    1. Top of page
    2. Original Article
    3. Case Report
    4. Letter to the Editor
    5. Announcement
    1. Multiple coagulation defects and the Cohen syndrome (pages 212–216)

      Tammi L. Schlichtemeier, Gail E. Tomlinson, Barton A. Kamen, Lewis J. Waber and Golder N. Wilson

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04026.x

  3. Letter to the Editor

    1. Top of page
    2. Original Article
    3. Case Report
    4. Letter to the Editor
    5. Announcement
    1. Achondroplasia with XXY karyotype (pages 217–218)

      B. S. Şayh, D. Gül and H. Çakirbay

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04027.x

  4. Announcement

    1. Top of page
    2. Original Article
    3. Case Report
    4. Letter to the Editor
    5. Announcement
    1. Announcement (page 219)

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04028.x

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