Clinical Genetics

Cover image for Vol. 75 Issue 4

April 2009

Volume 75, Issue 4

Pages 307–407

  1. Developmental Biology: Frontiers for Clinical Genetics

    1. Top of page
    2. Developmental Biology: Frontiers for Clinical Genetics
    3. HotSpots
    4. Commentary
    5. Original Articles
    6. Short Reports
    7. Letters to the Editor
    1. You have free access to this content
      Plumbing in the embryo: developmental defects of the urinary tracts (pages 307–317)

      N Uetani and M Bouchard

      Version of Record online: 15 APR 2009 | DOI: 10.1111/j.1399-0004.2009.01175.x

  2. HotSpots

    1. Top of page
    2. Developmental Biology: Frontiers for Clinical Genetics
    3. HotSpots
    4. Commentary
    5. Original Articles
    6. Short Reports
    7. Letters to the Editor
    1. PCSK1 variants: genetic risk factors for obesity (pages 318–319)

      SS Sanders

      Version of Record online: 15 APR 2009 | DOI: 10.1111/j.1399-0004.2009.01171_1.x

  3. Commentary

    1. Top of page
    2. Developmental Biology: Frontiers for Clinical Genetics
    3. HotSpots
    4. Commentary
    5. Original Articles
    6. Short Reports
    7. Letters to the Editor
    1. Gastroschisis: etiology and developmental pathogenesis (pages 322–325)

      KL Jones, K Benirschke and CD Chambers

      Version of Record online: 15 APR 2009 | DOI: 10.1111/j.1399-0004.2009.01164.x

  4. Original Articles

    1. Top of page
    2. Developmental Biology: Frontiers for Clinical Genetics
    3. HotSpots
    4. Commentary
    5. Original Articles
    6. Short Reports
    7. Letters to the Editor
    1. Escape of the yolk sac: a hypothesis to explain the embryogenesis of gastroschisis (pages 326–333)

      RE Stevenson, RC Rogers, JC Chandler, MWL Gauderer and AGW Hunter

      Version of Record online: 15 APR 2009 | DOI: 10.1111/j.1399-0004.2008.01142.x

    2. Germ line MLH1 and MSH2 mutations in Taiwanese Lynch syndrome families: characterization of a founder genomic mutation in the MLH1 gene (pages 334–345)

      R Tang, C Hsiung, J-Y Wang, C-H Lai, H-T Chien, L-L Chiu, C-T Liu, H-H Chen, H-M Wang, S-X Chen, L-L Hsieh and the TCOG HNPCC Consortium

      Version of Record online: 15 APR 2009 | DOI: 10.1111/j.1399-0004.2009.01162.x

    3. Penetrance and clinical consequences of a gross SDHB deletion in a large family (pages 354–363)

      DC Solis, N Burnichon, HJLM Timmers, MJ Raygada, A Kozupa, MJ Merino, D Makey, KT Adams, A Venisse, A-P Gimenez-Roqueplo and K Pacak

      Version of Record online: 7 APR 2009 | DOI: 10.1111/j.1399-0004.2009.01157.x

  5. Short Reports

    1. Top of page
    2. Developmental Biology: Frontiers for Clinical Genetics
    3. HotSpots
    4. Commentary
    5. Original Articles
    6. Short Reports
    7. Letters to the Editor
    1. You have free access to this content
      A functional network module for Smith–Magenis syndrome (pages 364–374)

      S Girirajan, HT Truong, CL Blanchard and SH Elsea

      Version of Record online: 19 FEB 2009 | DOI: 10.1111/j.1399-0004.2008.01135.x

    2. Omani-type spondyloepiphyseal dysplasia with cardiac involvement caused by a missense mutation in CHST3 (pages 375–383)

      B Tuysuz, S Mizumoto, K Sugahara, A Çelebi, S Mundlos and S Turkmen

      Version of Record online: 23 MAR 2009 | DOI: 10.1111/j.1399-0004.2009.01167.x

    3. Clinical features of microdeletion 9q22.3 (pat) (pages 384–393)

      K Shimojima, M Adachi, M Tanaka, Y Tanaka, K Kurosawa and T Yamamoto

      Version of Record online: 23 MAR 2009 | DOI: 10.1111/j.1399-0004.2008.01141.x

    4. Dominant versus recessive traits conveyed by allelic mutations – to what extent is nonsense-mediated decay involved? (pages 394–400)

      S Ben-Shachar, M Khajavi, MA Withers, CA Shaw, H Van Bokhoven, HG Brunner and JR Lupski

      Version of Record online: 19 FEB 2009 | DOI: 10.1111/j.1399-0004.2008.01114.x

  6. Letters to the Editor

    1. Top of page
    2. Developmental Biology: Frontiers for Clinical Genetics
    3. HotSpots
    4. Commentary
    5. Original Articles
    6. Short Reports
    7. Letters to the Editor
    1. Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta (pages 401–404)

      PS Hart, S Becerik, D Cogulu, G Emingil, D Ozdemir-Ozenen, ST Han, PP Sulima, E Firatli and TC Hart

      Version of Record online: 11 FEB 2009 | DOI: 10.1111/j.1399-0004.2008.01112.x

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