Clinical Genetics

Cover image for Clinical Genetics

August 1995

Volume 48, Issue 2

Pages 57–112

  1. Original Article

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Report on DNA Marker at Candidate Locus
    5. Letter to the Editor
    1. Tracheoesophageal anomalies in oculoauriculovertebral (Goldenhar) spectrum (pages 66–71)

      Rebecca Sutphen, Enrique Galan-Gomez, Xavier Cortada, Patricia N. Newkirk and Boris G. Kousseff

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04057.x

    2. Opitz BBBG syndrome: new family with late-onset, serious complication (pages 76–79)

      Jaap Schrander, Connie Schrander-Stumpel, Jelle Berg and Jaime L. Frias

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04059.x

    3. Noonan syndrome with café-au-lait spots and multiple lentigines syndrome are not linked to the neurofibromatosis type 1 locus (pages 85–89)

      Bodil Edman Ahlbom, Niklas Dahl, Per Zetterqvist and Goran Annerén

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04061.x

    4. Identification of the valine 408 to methionine mutation in the LDL receptor in a Greek patient with homozygous familial hypercholesterolemia (pages 90–92)

      H. Schuster, C. Manke, J. Fischer, C. Keller, G. Wolfram and N. Zöllnery

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04062.x

    5. Population frequency of apolipoprotein E5 (Glu3[RIGHTWARDS ARROW]Lys) and E7 (Glu244[RIGHTWARDS ARROW]Lys, Glu245[RIGHTWARDS ARROW]Lys) variants in western Japana (pages 93–99)

      Akira Matsunaga, Jun Sasaki, Kengo Moriyama, Fumiko Arakawa, Yoichi Takada, Kayo Nishi, Kazuko Hidaka and Kikuo Arakawa

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04063.x

  2. Case Report

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Report on DNA Marker at Candidate Locus
    5. Letter to the Editor
    1. Congenital heart disease in the 48,XXYY syndrome (pages 100–102)

      Dieter Meschede, Torsten Nekarda, Deniz Kececioglu, Hermann Löser, Johannes Vogt, Peter Miny and Jürgen Horst

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04064.x

    2. Clinical and molecular analysis of a Japanese boy with Morquio B disease (pages 103–108)

      Nozomi Ishii, Takahiko Oohira, Akihiro Oshima, Hitoshi Sakuraba, Fumio Endo, Ichiro Matsuda, Kazuko Sukegawa, Tadao Orii and Yoshiyuki Suzuki

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04065.x

  3. Short Report on DNA Marker at Candidate Locus

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Report on DNA Marker at Candidate Locus
    5. Letter to the Editor
    1. The Pvull restriction site in the second intron of the human steroid 21-hydroxylase gene CYP21 is polymorphic (pages 109–110)

      Paul F. J. Koppens, Theo Hoogenboezem and Herman J. Degenhart

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04066.x

  4. Letter to the Editor

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Report on DNA Marker at Candidate Locus
    5. Letter to the Editor

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