Clinical Genetics

Cover image for Clinical Genetics

May 1994

Volume 45, Issue 5

Pages 221–276

  1. Original Article

    1. Top of page
    2. Original Article
    3. Letter to the Editor
    4. Announcement
    1. Familial occurrence of Hirschsprung's disease (pages 231–235)

      Michael Bjern Russell, Charlotte Astrid Russell, Kirsten Fenger and Erik Niebuhr

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04147.x

    2. DNA carrier detection in X-linked progressive cone dystrophy (pages 236–240)

      A. A. B. Bergen, F. Meire, E. J. M. Schuurman and J. W. Delleman

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04148.x

    3. Linkage analysis of 62 X-chromosomal loci excludes the X chromosome in an Icelandic family showing apparent X-linked recessive inheritance of neural tube defects (pages 241–249)

      R. Newton, P. Stanier, S. Loughna, D. J. Henderson, S. A. Forbes, M. Farrall, O. Jensson and G. E. Moore

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04149.x

    4. Umbilical findings in Aarskog syndrome (pages 260–265)

      Masato Tsukahara and G. Isabel Fernandez

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04152.x

    5. Allele frequencies of Mp6D-9 and GATT markers in 32 Turkish cystic fibrosis families (pages 266–268)

      M. Özgüç, E. Yilmaz, H. Erdem, T. Coşkun, U. Özçelik, I. Togan, A. Göçmen, S. Ayter and I. Özalp

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04153.x

  2. Letter to the Editor

    1. Top of page
    2. Original Article
    3. Letter to the Editor
    4. Announcement
    1. Pitted enamel hypoplasia in tuberous sclerosis (page 269)

      David Webb, John P. Osborne and Antonia Clarke

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04154.x

    2. Video display terminal — the risk of trisomy 18? (pages 270–271)

      Nilgun Kultursay, Ferda Koprubasi and Necil Kutukculer

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04155.x

    3. Currarino triad (anorectal malformation, sacral bony abnormality and presacral mass) with partial trisomy of chromosomes 13q and 20p (pages 272–273)

      Toshiro Nagai, Rumiko Katoh, Tomonobu Hasegawa, Hirofumi Ohashi and Yoshimitsu Fukushima

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04156.x

    4. Rett syndrome: random X chromosome inactivation (pages 274–275)

      Maria Anvret and Jan Wahlström

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04157.x

  3. Announcement

    1. Top of page
    2. Original Article
    3. Letter to the Editor
    4. Announcement
    1. Announcements (page 276)

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1994.tb04158.x

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