Clinical Genetics

Cover image for Clinical Genetics

July 1986

Volume 30, Issue 1

Pages 1–80

  1. Original Article

    1. Top of page
    2. Original Article
    3. Letter to the Editors
    1. Dermatoglyphic peculiarities in families with X-linked mental retardation and fragile site Xq27: a collaborative study (pages 1–13)

      A. Rodewald, U. Froster-Iskenius, E. Kab, U. Langenbeck, A. Schinzel, A. Schmidt, E. Schwinger, P. Steinbach, H. Veenema, R.-D. Wegner, A. Wirtz, H. Zankl and M. Zankl

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00563.x

    2. Usher syndrome in four Norwegian counties (pages 14–28)

      Jan Grøndahl and Svein Mjøen

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00564.x

    3. Adult polycystic liver and kidney diseases are separate entities (pages 29–37)

      PekkaJ. Karhunen and Martti Tenhu

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00565.x

    4. Relative reliability of three different discriminant analysis methods for detecting PKU gene carriers (pages 38–40)

      S. L. Wenger, P. W. Vieira, J. M. Breck and M. W. Steele

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00566.x

    5. Number of “high genes” involved in determining the activity of paraoxonase (pages 41–49)

      Arne Nielsen, Hans Eiberg, Kirsten Fenger and Jan Mohr

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00567.x

    6. Partial trisomy 3p syndrome (pages 50–58)

      JacobA. Reiss, LesJ. Sheffield and GrantR. Sutherland

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00568.x

    7. Structure, origin and effects of a supernumerary marker chromosome 15 (pages 63–71)

      M. Schmid, D. Schindler and T. HAAF

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00570.x

    8. Autosomal whole arm translocations in man : A patient with t(5p7p;5q7q) type rearrangement and review of the literature (pages 72–75)

      Alice Kleczkowska, Jean-Pierre Fryns and HermanVanDen Berghe

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00571.x

    9. Paternal non-disjunction in a 46, XY/ 47, XXY individual with a fragile 17p12 in the mother (pages 76–79)

      N. TOMMERUP, T. TøNNESEN and K. -H. GUSTAVSON

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00572.x

  2. Letter to the Editors

    1. Top of page
    2. Original Article
    3. Letter to the Editors
    1. An unusual variant chromosome 9 due to disturbance of normal chromatin condensation at band p12? (page 80)

      Mahmoud Djalali, Gotthold Barbi and Peter Steinbach

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00573.x

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