Clinical Genetics

Cover image for Clinical Genetics

January 2005

Volume 67, Issue 1

Pages 1–106

  1. Review Articles

    1. Top of page
    2. Review Articles
    3. HotSpots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. Studying the genetics of Hirschsprung's disease: unraveling an oligogenic disorder (pages 6–14)

      AS Brooks, BA Oostra and RMW Hofstra

      Version of Record online: 21 SEP 2004 | DOI: 10.1111/j.1399-0004.2004.00319.x

    2. The endless quest for sex determination genes (pages 15–25)

      A Fleming and E Vilain

      Version of Record online: 11 NOV 2004 | DOI: 10.1111/j.1399-0004.2004.00376.x

  2. HotSpots

    1. Top of page
    2. Review Articles
    3. HotSpots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. Mutations in TGF-β receptor type-2 cause Marfan's syndrome (pages 26–27)

      JR Helm and MLE MacDonald

      Version of Record online: 11 NOV 2004 | DOI: 10.1111/j.1399-0004.2004.0375a.x

    2. RNAi applied to a neurodegenerative mouse model (pages 27–29)

      JR Helm

      Version of Record online: 11 NOV 2004 | DOI: 10.1111/j.1399-0004.2004.0375b.x

  3. Original Articles

    1. Top of page
    2. Review Articles
    3. HotSpots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. Evidence for single origins of 35delG and delE120 mutations in the GJB2 gene in Anatolia (pages 31–37)

      M Tekin, G Boğoclu, ST Arican, MN Orman, H Tastan, S Elsayed and N Akar

      Version of Record online: 20 OCT 2004 | DOI: 10.1111/j.1399-0004.2004.00334.x

    2. FMR1 alleles in Tasmania: a screening study of the special educational needs population (pages 38–46)

      RJ Mitchell, JJA Holden, C Zhang, Y Curlis, HR Slater, T Burgess, KC Kirkby, A Carmichael, KD Heading and DZ Loesch

      Version of Record online: 20 OCT 2004 | DOI: 10.1111/j.1399-0004.2004.00344.x

    3. The Hunter–McAlpine syndrome results from duplication 5q35–qter (pages 53–60)

      AGW Hunter, B Dupont, M McLaughlin, L Hinton, E Baker, L Adès, E Haan and CE Schwartz

      Version of Record online: 22 DEC 2004 | DOI: 10.1111/j.1399-0004.2005.00378.x

  4. Short Reports

    1. Top of page
    2. Review Articles
    3. HotSpots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non-syndromic hearing impairment (pages 61–68)

      RLP Santos, M Wajid, TL Pham, J Hussan, G Ali, W Ahmad and SM Leal

      Version of Record online: 22 DEC 2004 | DOI: 10.1111/j.1399-0004.2005.00379.x

    2. A novel STK11 germline mutation in two siblings with Peutz–Jeghers syndrome complicated by primary gastric cancer (pages 81–86)

      K Shinmura, M Goto, H Tao, S Shimizu, Y Otsuki, H Kobayashi, S Ushida, K Suzuki, T Tsuneyoshi and H Sugimura

      Version of Record online: 22 DEC 2004 | DOI: 10.1111/j.1399-0004.2005.00380.x

    3. Psychiatric and neuropsychological characterization of Pallister-Hall syndrome (pages 87–92)

      A Azzam, DM Lerner, KF Peters, E Wiggs, DL Rosenstein and LG Biesecker

      Version of Record online: 22 DEC 2004 | DOI: 10.1111/j.1399-0004.2005.00370.x

    4. Fine mapping of the X-linked split-hand/split-foot malformation (SHFM2) locus to a 5.1-Mb region on Xq26.3 and analysis of candidate genes (pages 93–97)

      M Faiyaz-Ul-Haque, SHE Zaidi, LM King, S Haque, M Patel, M Ahmad, T Siddique, W Ahmad, L-C Tsui and DH Cohn

      Version of Record online: 25 OCT 2004 | DOI: 10.1111/j.1399-0004.2004.00369.x

  5. Letters to the Editor

    1. Top of page
    2. Review Articles
    3. HotSpots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. A dramatic case of early-onset familial adenomatous polyposis (pages 104–106)

      R Auricchio, M De Rosa, L Quaglietta, E Miele, G Boccia, A Staiano and P Izzo

      Version of Record online: 22 DEC 2004 | DOI: 10.1111/j.1399-0004.2005.00381.x

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