Clinical Genetics

Cover image for Clinical Genetics

September 2007

Volume 72, Issue 3

Pages 167–270

  1. Review

    1. Top of page
    2. Review
    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. Review
    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. Review
    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. Review
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. HotSpots
    5. Original Articles
    6. Short Reports
    7. Letters to the Editor
    1. Development and testing of a decision aid for breast cancer prevention for women with a BRCA1 or BRCA2 mutation (pages 208–217)

      KA Metcalfe, A Poll, A O’Connor, S Gershman, S Armel, A Finch, R Demsky, B Rosen and SA Narod

      Version of Record online: 9 AUG 2007 | DOI: 10.1111/j.1399-0004.2007.00859.x

  5. Short Reports

    1. Top of page
    2. Review
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. HotSpots
    5. Original Articles
    6. Short Reports
    7. Letters to the Editor
    1. Cystic fibrosis in a southern Brazilian population: characteristics of 90% of the alleles (pages 218–223)

      FR Faucz, J Gimenez, MD Ramos, L Pereira-Ferrari, X Estivill, S Raskin, T Casals and L Culpi

      Version of Record online: 27 JUL 2007 | DOI: 10.1111/j.1399-0004.2007.00854.x

    2. CYR61 polymorphisms are associated with plasma HDL-cholesterol levels in obese individuals (pages 224–229)

      L Bouchard, A Tchernof, Y Deshaies, S Lebel, F-S Hould, P Marceau and M-C Vohl

      Version of Record online: 27 JUL 2007 | DOI: 10.1111/j.1399-0004.2007.00855.x

    3. Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCC (pages 230–237)

      B Roncari, M Pedroni, S Maffei, C Di Gregorio, G Ponti, A Scarselli, L Losi, P Benatti, L Roncucci, C De Gaetani, L Camellini, E Lucci-Cordisco, R Tricarico, M Genuardi and M Ponz de Leon

      Version of Record online: 6 AUG 2007 | DOI: 10.1111/j.1399-0004.2007.00856.x

    4. Detection of copy number changes at the NF1 locus with improved high-resolution array CGH (pages 238–244)

      MH Shen, K Mantripragada, JP Dumanski, I Frayling and M Upadhyaya

      Version of Record online: 13 AUG 2007 | DOI: 10.1111/j.1399-0004.2007.00858.x

    5. A distinct spectrum of SLC26A4 mutations in patients with enlarged vestibular aqueduct in China (pages 245–254)

      Q-J Wang, Y-L Zhao, S-Q Rao, Y-F Guo, H Yuan, L Zong, J Guan, B-C Xu, D-Y Wang, M-K Han, L Lan, S-Q Zhai and Y Shen

      Version of Record online: 13 AUG 2007 | DOI: 10.1111/j.1399-0004.2007.00862.x

    6. Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucoma (pages 255–260)

      DP Dimasi, AW Hewitt, T Straga, J Pater, JR MacKinnon, JE Elder, T Casey, DA Mackey and JE Craig

      Version of Record online: 6 AUG 2007 | DOI: 10.1111/j.1399-0004.2007.00864.x

  6. Letters to the Editor

    1. Top of page
    2. Review
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. HotSpots
    5. Original Articles
    6. Short Reports
    7. Letters to the Editor
    1. Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families (pages 261–263)

      M Hashemzadeh Chaleshtori, MA Simpson, E Farrokhi, M Dolati, L Hoghooghi Rad, S Amani Geshnigani and AH Crosby

      Version of Record online: 27 JUL 2007 | DOI: 10.1111/j.1399-0004.2007.00852.x

    2. Frequency of hemochromatosis gene (HFE) mutations in Corsica (France) (pages 268–270)

      I Piras, A Melis, A Falchi, L Varesi, CM Calò and G Vona

      Version of Record online: 27 JUL 2007 | DOI: 10.1111/j.1399-0004.2007.00857.x

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