Clinical Genetics

Cover image for Clinical Genetics

March 1979

Volume 15, Issue 3

Pages 209–287

  1. Original Article

    1. Top of page
    2. Original Article
    3. Announcement
    1. Acrocephalopolysyndactyly type IV: A new genetic syndrome in 3 sibs (pages 209–214)

      R. M. Goodman, M. Sternberg, Y. Shem-Tov, M. Bat-Miriam Katznelson, M. Hertz and Y. Rotem

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00969.x

    2. The human X-chromosome and the levels of serum immunoglobulin M (pages 221–227)

      Victor Escobar, Linda A. Corey, David Bixler, Walter E. Nance and Angenieta Biegei

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00971.x

    3. X-linked dominant ichthyosis (pages 239–240)

      Rudolf Happle

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00973.x

    4. Familial occurrence of syngnathia congenita syndrome (pages 241–244)

      I. Gassner, W. Müller, H. Rössler, J. Kofler and G. Mitterstieler

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00974.x

    5. Regional mapping of the HLA on the short arm of chromosome 6 (pages 245–251)

      R. Berger, A. Bernheim, M. Sasportes, G. Hauptmann, J. Hors, L. Legrand and M. Fellous

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00975.x

    6. Craniometaphyseal dysplasia -variability of expression within a large family (pages 252–258)

      Peter Beighton, Herman Hamersma and Frank Horan

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00976.x

    7. Turner's syndrome with a duplication-deficiency X chromosome derived from a maternal pericentric inversion X chromosome (pages 259–266)

      Tohru Maeda, Michiko Ohno, Masumi Takada, Masato Nishida, Kazuko Tsukioka and Hajime Tomjta

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00977.x

    8. Prenatal diagnosis of trisomy 20 mosaicism (pages 267–272)

      Nataline B. Kardon, Ernest Lieber, Jessica G. Davis and Lillian Y. F. Hsu

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00978.x

    9. Prenatal diagnosis of polycystic kidneys and encephalocele (Meckel syndrome) (pages 278–286)

      U. Friedrich, K. Brogård Hansen, M. Hauge, I. Hägerstrand, K. Kristoffersen, E. Ludvigsen, U. Merrild, B. Nørgaard-Pedersen, G. Bruun Petersen and A. J. Therkelsen

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00980.x

  2. Announcement

    1. Top of page
    2. Original Article
    3. Announcement
    1. Announcement (page 287)

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00981.x

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