Clinical Genetics

Cover image for Clinical Genetics

April 2006

Volume 69, Issue 4

Pages 297–370

  1. Perspectives

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

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

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

    1. Top of page
    2. Perspectives
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. HotSpots
    5. Original Articles
    6. Short Reports
    7. Letters to the Editor
    1. Clinical profiles of four patients with Rett syndrome carrying a novel exon 1 mutation or genomic rearrangement in the MECP2 gene (pages 319–326)

      D Bartholdi, A Klein, M Weissert, N Koenig, A Baumer, E Boltshauser, A Schinzel, W Berger and G Mátyás

      Version of Record online: 30 MAR 2006 | DOI: 10.1111/j.1399-0004.2006.00604.x

  5. Short Reports

    1. Top of page
    2. Perspectives
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. HotSpots
    5. Original Articles
    6. Short Reports
    7. Letters to the Editor
    1. A successful approach for the detection of Fabry patients in Argentina (pages 344–348)

      PA Rozenfeld, A Tarabuso, R Ebner, G Ramallo and CA Fossati

      Version of Record online: 30 MAR 2006 | DOI: 10.1111/j.1399-0004.2006.00594.x

    2. LADD syndrome is caused by FGF10 mutations (pages 349–354)

      JM Milunsky, G Zhao, TA Maher, R Colby and DB Everman

      Version of Record online: 30 MAR 2006 | DOI: 10.1111/j.1399-0004.2006.00597.x

  6. Letters to the Editor

    1. Top of page
    2. Perspectives
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. HotSpots
    5. Original Articles
    6. Short Reports
    7. Letters to the Editor
    1. Skin abnormalities as an early predictor of neurologic outcome in Gaucher disease (pages 355–357)

      WM Holleran, SG Ziegler, O Goker-Alpan, MJ Eblan, PM Elias, R Schiffmann and E Sidransky

      Version of Record online: 6 MAR 2006 | DOI: 10.1111/j.1399-0004.2006.00589.x

    2. Paraoxonase-1 Q192R polymorphism and risk of sporadic amyotrophic lateral sclerosis (pages 358–359)

      A Slowik, B Tomik, D Partyka, W Turaj, J Pera, T Dziedzic, P Szermer, DA Figlewicz and A Szczudlik

      Version of Record online: 6 MAR 2006 | DOI: 10.1111/j.1399-0004.2006.00590.x

    3. The incidence patterns of Down syndrome in Qatar (pages 360–362)

      Atiqa Abdul Wahab, Abdulbari Bener and Ahmad S. Teebi

      Version of Record online: 30 MAR 2006 | DOI: 10.1111/j.1399-0004.2006.00593.x

    4. Identification of a submicroscopic deletion of SHH associated with the holoprosencephaly spectrum by array-based CGH (pages 367–369)

      Jia Huang, Jodi D. Hoffman, Yi Zhang, Melissa K. Maisenbacher, Elaine H. Zackai, Barbara L. Weber and Jeffrey E. Ming

      Version of Record online: 30 MAR 2006 | DOI: 10.1111/j.1399-0004.2006.00598.x

    5. You have free access to this content
      Erratum (page 370)

      Version of Record online: 30 MAR 2006 | DOI: 10.1111/j.1399-0004.2006.00610.x

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