Clinical Genetics

Cover image for Clinical Genetics

January 2007

Volume 71, Issue 1

Pages 1–99

  1. Reviews

    1. Top of page
    2. Reviews
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. Social and Behavioural Research in Clinical Genetics
    5. HotSpots
    6. Original Articles
    7. Short Reports
    8. Letters to the Editor
    9. Corrigendum
    1. The modular nature of genetic diseases (pages 1–11)

      M Oti and HG Brunner

      Version of Record online: 17 OCT 2006 | DOI: 10.1111/j.1399-0004.2006.00708.x

    2. Diagnosis and management of early- and late-onset cerebellar ataxia (pages 12–24)

      E Brusse, JA Maat-Kievit and JC Van Swieten

      Version of Record online: 28 NOV 2006 | DOI: 10.1111/j.1399-0004.2006.00722.x

  2. Developmental Biology: Frontiers for Clinical Genetics

    1. Top of page
    2. Reviews
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. Social and Behavioural Research in Clinical Genetics
    5. HotSpots
    6. Original Articles
    7. Short Reports
    8. Letters to the Editor
    9. Corrigendum
  3. Social and Behavioural Research in Clinical Genetics

    1. Top of page
    2. Reviews
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. Social and Behavioural Research in Clinical Genetics
    5. HotSpots
    6. Original Articles
    7. Short Reports
    8. Letters to the Editor
    9. Corrigendum
    1. Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study (pages 35–42)

      I Van Oostrom, H Meijers-Heijboer, HJ Duivenvoorden, AHJT Bröcker-Vriends, CJ Van Asperen, RH Sijmons, C Seynaeve, AR Van Gool, JGM Klijn and A Tibben

      Version of Record online: 14 DEC 2006 | DOI: 10.1111/j.1399-0004.2007.00731.x

  4. HotSpots

    1. Top of page
    2. Reviews
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. Social and Behavioural Research in Clinical Genetics
    5. HotSpots
    6. Original Articles
    7. Short Reports
    8. Letters to the Editor
    9. Corrigendum
  5. Original Articles

    1. Top of page
    2. Reviews
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. Social and Behavioural Research in Clinical Genetics
    5. HotSpots
    6. Original Articles
    7. Short Reports
    8. Letters to the Editor
    9. Corrigendum
    1. The correlation of CTG repeat length with material and social deprivation in myotonic dystrophy (pages 59–66)

      L Laberge, S Veillette, J Mathieu, J Auclair and M Perron

      Version of Record online: 14 DEC 2006 | DOI: 10.1111/j.1399-0004.2007.00732.x

    2. Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasia (pages 67–75)

      M Leipoldt, M Erdel, GA Bien-Willner, M Smyk, M Theurl, SA Yatsenko, JR Lupski, AH Lane, AL Shanske, P Stankiewicz and G Scherer

      Version of Record online: 14 DEC 2006 | DOI: 10.1111/j.1399-0004.2007.00736.x

  6. Short Reports

    1. Top of page
    2. Reviews
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. Social and Behavioural Research in Clinical Genetics
    5. HotSpots
    6. Original Articles
    7. Short Reports
    8. Letters to the Editor
    9. Corrigendum
    1. In search of a familial cancer risk assessment tool (pages 76–83)

      KM Kelly and K Sweet

      Version of Record online: 28 NOV 2006 | DOI: 10.1111/j.1399-0004.2006.00728.x

    2. Co-existence of two functional mutations on the same allele of the human ferrochelatase gene in erythropoietic protoporphyria (pages 84–88)

      E Di Pierro, V Brancaleoni, V Moriondo, V Besana and MD Cappellini

      Version of Record online: 14 DEC 2006 | DOI: 10.1111/j.1399-0004.2007.00733.x

  7. Letters to the Editor

    1. Top of page
    2. Reviews
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. Social and Behavioural Research in Clinical Genetics
    5. HotSpots
    6. Original Articles
    7. Short Reports
    8. Letters to the Editor
    9. Corrigendum
    1. Early lethal autosomal recessive enterocolitis: report of a second family (pages 89–90)

      A. Mégarbané and R. Sayad

      Version of Record online: 14 DEC 2006 | DOI: 10.1111/j.1399-0004.2007.00735.x

    2. ENG mutations in MADH4/BMPR1A mutation negative patients with juvenile polyposis (pages 91–92)

      JR Howe, JL Haidle, G Lal, J Bair, C Song, B Pechman, S Chinnathambi and HT Lynch

      Version of Record online: 14 DEC 2006 | DOI: 10.1111/j.1399-0004.2007.00734.x

    3. Inheritance of a novel RYR1 mutation in a family with myotonic dystrophy type 1 (pages 93–94)

      S Gambelli, A Malandrini, G Berti, C Gaudiano, E Zicari, P Brunori, G Perticoni, A Orrico, L Galli, V Sorrentino, J Lunardi, A Federico and MT Dotti

      Version of Record online: 28 NOV 2006 | DOI: 10.1111/j.1399-0004.2006.00725.x

    4. Six novel mutations in the GCK gene in MODY patients (pages 95–96)

      D Pinterova, J Ek, K Kolostova, S Pruhova, P Novota, M Romzova, E Feigerlova, M Cerna, J Lebl, O Pedersen and T Hansen

      Version of Record online: 28 NOV 2006 | DOI: 10.1111/j.1399-0004.2006.00729.x

  8. Corrigendum

    1. Top of page
    2. Reviews
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. Social and Behavioural Research in Clinical Genetics
    5. HotSpots
    6. Original Articles
    7. Short Reports
    8. Letters to the Editor
    9. Corrigendum
    1. You have free access to this content
      Corrigendum (page 99)

      Version of Record online: 14 DEC 2006 | DOI: 10.1111/j.1399-0004.2007.00744.x

      This article corrects:

      Predictive testing for Huntington disease: interpretation and significance of intermediate alleles

      Vol. 70, Issue 4, 283–294, Version of Record online: 21 AUG 2006

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