Clinical Genetics

Cover image for Clinical Genetics

August 1985

Volume 28, Issue 2

Pages 97–183

  1. Original Article

    1. Top of page
    2. Original Article
    3. Short Communication
    4. Letters to the Editors
    5. Announcements
    1. Frequency of fragile X chromosome in normal females (pages 97–99)

      Dunne Abuelo, Katherine Castree, Siegfried Pueschel, Teresita Padre-Mendoza and Kathy Zolnierz

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00366.x

    2. Age of onset in siblings of persons with juvenile Huntinqton disease (pages 100–105)

      M. R. Hayden, J. A. Soles and D R. H. Ward

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00367.x

    3. Heterogeneity of Kallmann's syndrome (pages 106–111)

      M. Hermanussen and W. G. Sippell

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00368.x

    4. Partial trisomy 12q: clinical and cytogenetic observations (pages 112–117)

      C. Tengström, M. Wilska, M. Kähkönen, S. Autio and J. Leisti

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00369.x

    5. The cerebro-costo-mandibular syndrome: third report of familial occurrence (pages 118–121)

      R. C. M. Hennekam, F. A. Beemer, W. A. R. Huijbers, P. A. Hustinx and F. J. van Sprang

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00370.x

    6. Partial trisomy 5q and partial monosomy 5q within the same family (pages 122–129)

      G. I. Lazjuk, I. W. Lurie, I. A. Kirillova, D. V. Zaletajev, D. B. Gurevich, I. A. Shved and T. I. Ostrovskaya

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00371.x

    7. EEC syndrome without ectrodactyly? Report of 8 cases (pages 130–135)

      W. Küster, F. Majewski and P. Meinecke

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00372.x

    8. Expression of X-linked hypohidrotic ectodermal dysplasia in six males and in their mothers (pages 136–144)

      Anna-Lisa Söderholm and Ilkka Kaitila

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00373.x

    9. Heritable fragility at 11q13 and 12q13 (pages 145–150)

      D. F. C. M. Smeets, J. M. J. C. Scheres and T. W. J. Hustinx

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00374.x

    10. Duchenne-like muscular dystrophy in two sisters with normal karyotypes: evidence for autosomal recessive inheritance (pages 151–156)

      Hannu Somer, Arja Voutilainen, Sakari Knuutila, Ilkka Kaitila, Juhani Rapola and Hannu Leinonen

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00375.x

    11. Cornelia de Lange syndrome in a mother and daughter (pages 157–161)

      Anne Leavitt, Nuhad Dinno and Catherine Davis

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00376.x

    12. An unusual variant chromosome 9 with an extra C-negative, G-dark segment in the short arm (pages 162–165)

      F. S. Spedicato, A. Di Comite and M. Tohidast-Akrad

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00377.x

    13. A complex structural rearrangement of chromosome 4 in a woman without phenotypic features of Wolf-Hirschhorn syndrome (pages 166–172)

      D. R. Romain, L. M. Columbano-Green, R. G. Parfitt, C. J. Chapman, R. H. Smythe and O. B. Gebbie

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00378.x

  2. Short Communication

    1. Top of page
    2. Original Article
    3. Short Communication
    4. Letters to the Editors
    5. Announcements
    1. A new banding pattern of human chromosomes by in situ nick translation using ECO RI and biotin-dUTP (pages 173–176)

      Jörn Bullerdiek, Jürgen Dittmer, Angelika Faehre, Sabine Bartnitzke, Volker Kasche and Werner Schloot

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00379.x

  3. Letters to the Editors

    1. Top of page
    2. Original Article
    3. Short Communication
    4. Letters to the Editors
    5. Announcements
    1. About diploid-tetraploid mosaicism (page 177)

      Y. Chamla

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00380.x

    2. 46, X, i(Xq) karyotype in a patient with hypoplastic left heart (pages 178–179)

      Ashok Shah, John E. Fay, Sally Ford and Jeanette J. A. Holden

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00381.x

    3. Imaging techniques in muscular dystrophies (pages 179–180)

      Hans-Dieter Rott and Werner Rödl

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00382.x

    4. Prenatal testing and twinning (pages 180–182)

      David B. Flannery and Gerald B. Holzman

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00383.x

  4. Announcements

    1. Top of page
    2. Original Article
    3. Short Communication
    4. Letters to the Editors
    5. Announcements

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