Clinical Genetics

Cover image for Clinical Genetics

March 2004

Volume 65, Issue 3

Pages 163–246

  1. Developmental Biology: Frontiers for Clinical Genetics

    1. Top of page
    2. Developmental Biology: Frontiers for Clinical Genetics
    3. Hotspots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
  2. Hotspots

    1. Top of page
    2. Developmental Biology: Frontiers for Clinical Genetics
    3. Hotspots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
  3. Original Articles

    1. Top of page
    2. Developmental Biology: Frontiers for Clinical Genetics
    3. Hotspots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. Concordance of phenotypic expression and gender identity in a large kindred with a mutation in the androgen receptor (pages 183–190)

      HT Hooper, BC Figueiredo, CC Pavan-Senn, L De Lacerda, R Sandrini, JK Mengarelli, K Japp and LP Karaviti

      Version of Record online: 30 JAN 2004 | DOI: 10.1111/j.0009-9163.2004.00197.x

    2. Polymorphisms in cytokines and growth factor genes and their association with acute rejection and recurrence of hepatitis C virus disease in liver transplantation (pages 191–201)

      VR Mas, a,b RA Fisher, c DG Maluf, c KJ Archer, d,e MJ Contos, a SA Mills, a ML Shiffman, f DS Wilkinson, a L Oliveros, d CT Garrett and a A Ferreira-Gonzalez a

      Version of Record online: 30 JAN 2004 | DOI: 10.1111/j.0009-9163.2004.00208.x

  4. Short Reports

    1. Top of page
    2. Developmental Biology: Frontiers for Clinical Genetics
    3. Hotspots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease (pages 209–214)

      YR Wu, HY Lin, CM Chen, K Gwinn-Hardy, LS Ro, YC Wang, SH Li, JC Hwang, K Fang, HM Hsieh-Li, ML Li, LC Tung, MT Su, KT Lu and GJ Lee-Chen

      Version of Record online: 30 JAN 2004 | DOI: 10.1111/j.0009-9163.2004.00213.x

    2. Hereditary non-polyposis colorectal cancer and the role of hPMS2 and hEXO1 mutations (pages 215–225)

      E Thompson, CJ Meldrum, R Crooks, M McPhillips, L Thomas, AD Spigelman and RJ Scott

      Version of Record online: 30 JAN 2004 | DOI: 10.1111/j.1399-0004.2004.00214.x

    3. The clinical picture of the Börjeson–Forssman–Lehmann syndrome in males and heterozygous females with PHF6 mutations (pages 226–232)

      G Turner, KM Lower, SM White, M Delatycki, AK Lampe, M Wright, J Clayton- Smith, B Kerr, S Schelley, HE Hoyme, BBA De Vries, T Kleefstra, M Grompe, B Cox, J Gecz and M Partington

      Version of Record online: 30 JAN 2004 | DOI: 10.1111/j.0009-9163.2004.00215.x

    4. Effective long-term control of cardiac events with β-blockers in a family with a common LQT1 mutation (pages 233–241)

      H Wedekind, M Schwarz, S Hauenschild, H Djonlagic, W Haverkamp, G Breithardt, T Wülfing, O Pongs, D Isbrandt and E Schulze-Bahr

      Version of Record online: 30 JAN 2004 | DOI: 10.1111/j.0009-9163.2004.00221.x

  5. Letters to the Editor

    1. Top of page
    2. Developmental Biology: Frontiers for Clinical Genetics
    3. Hotspots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. Supernumerary marker 15 chromosome in a patient with Prader–Willi syndrome (pages 242–243)

      D Borelina, S Esperante, V Gutnisky, V Ferreiro, M Ferrer, F Giliberto, G Frechtel, L Francipane and I Szijan

      Version of Record online: 30 JAN 2004 | DOI: 10.1111/j.0009-9163.2004.00203.x

    2. Heterozygous manifestations in female carriers of Mal de Meleda (pages 244–246)

      M Mokni, C Charfeddine, R Ben Mously, D Baccouche, B Kaabi, A Ben Osman, K Dellagi and S Abdelhak

      Version of Record online: 30 JAN 2004 | DOI: 10.1111/j.0009-9163.2004.00224.x

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