Clinical Genetics

Cover image for Clinical Genetics

February 1979

Volume 15, Issue 2

Pages 113–207

  1. Original Article

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    4. Announcements
    1. Prenatal monitoring for the Hunter syndrome: The heterozygous female fetus (pages 113–117)

      W. J. KLEIJER, P. D. MOOY, I. LIEBAERS, J. J. P. VAN DE KAMP and M. F. NIERMEIJER

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01749.x

    2. Autosomal recessive onychotrichodysplasia, chronic neutropenia and mild mental retardation : Delineation of the syndrome (pages 147–152)

      Alejandro Hernández, Francisco Olivares and José-María Cantú

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01753.x

    3. Trisomy 20q due to maternal t(16;20) translocation First case (pages 167–170)

      I. H. Pawlowitzki, H. Gröbe and W. Holzgreve

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01756.x

    4. Partial trisomy 13 plus partial trisomy 4q due to unusual segregation of translocation chromosomes (pages 176–182)

      Christa Fonatsch, Sibylle D. Flatz and Eva Weitzel

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01758.x

    5. Glucose-6-phosphate dehydrogenase deficiency in Sicily. Incidence, biochemical characteristics and clinical implications (pages 183–188)

      G. Schiliro, A. Russo, R. Curreri, S. Marino, A. Sciotto and G. Russo

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01759.x

    6. Melkersson- Rosenthal's syndrome in four generations (pages 189–192)

      C. Lygidakis, C. Tsakanikas, A. Ilias and D. Vassilopoulos

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01760.x

    7. C-band polymorphism in human chromosome no. 6 (pages 193–197)

      K. Madan and A. H. Bruinsma

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01761.x

    8. Orientation of major histocompatibility (MHC) genes relative to the centromere of human chromosome 6 (pages 198–202)

      E. Barker, P. L. Pearson, P. Meera Khan, G. M. TH. Schreuder and K. Madan

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01762.x

  2. Letters to the Editors

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    4. Announcements
    1. Familial holoprosencephaly (pages 203–204)

      Victor Escobar and Jose Maria Cantu

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01763.x

    2. Reply to Escobar and Cantu (pages 204–205)

      Alice O. Martin

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01764.x

    3. “Adult” form of polycystic kidney disease in neonates (pages 205–206)

      J. P. Fryns and H. Van Den Berghe

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01765.x

    4. Ichthyosis vulgaris (page 206)

      Naomi Fitch

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01766.x

  3. Announcements

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    4. Announcements
    1. Announcements (page 207)

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01767.x

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