Clinical Genetics

Cover image for Clinical Genetics

July 2007

Volume 72, Issue 1

Pages 1–65

  1. Developmental Biology: Frontiers for Clinical Genetics

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

    1. Top of page
    2. Developmental Biology: Frontiers for Clinical Genetics
    3. HotSpots
    4. Short Reports
    5. Letters to the Editor
    1. Cognition genes on autosomes: the paradox (pages 9–12)

      PJ Willems

      Version of Record online: 10 JUN 2007 | DOI: 10.1111/j.1399-0004.2007.00823.x

  3. Short Reports

    1. Top of page
    2. Developmental Biology: Frontiers for Clinical Genetics
    3. HotSpots
    4. Short Reports
    5. Letters to the Editor
    1. Executive functioning in children and adolescents with phenylketonuria (pages 13–18)

      KH VanZutphen, W Packman, L Sporri, MC Needham, C Morgan, K Weisiger and S Packman

      Version of Record online: 26 JUN 2007 | DOI: 10.1111/j.1399-0004.2007.00816.x

    2. Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11–q21.32 (pages 23–29)

      A Wali, MS Chishti, M Ayub, M Yasinzai, , G Ali, P John and W Ahmad

      Version of Record online: 27 MAY 2007 | DOI: 10.1111/j.1399-0004.2007.00818.x

    3. Large deletions in the CFTR gene: clinics and genetics in Swiss patients with CF (pages 30–38)

      M Schneider, C Hirt, C Casaulta, J Barben, R Spinas, U Bühlmann, J Spalinger, B Schwizer, F Chevalier-Porst and S Gallati

      Version of Record online: 10 JUN 2007 | DOI: 10.1111/j.1399-0004.2007.00820.x

    4. Does cystic fibrosis neonatal screening detect atypical CF forms? Extended genetic characterization and 4-year clinical follow-up (pages 39–46)

      L Narzi, G Ferraguti, A Stamato, F Narzi, SB Valentini, A Lelli, I Delaroche, M Lucarelli, R Strom and S Quattrucci

      Version of Record online: 26 JUN 2007 | DOI: 10.1111/j.1399-0004.2007.00825.x

    5. 17p11.2p12 triplication and del(17)q11.2q12 in a severely affected child with dup(17)p11.2p12 syndrome (pages 47–58)

      S Girirajan, SR Williams, JY Garbern, N Nowak, E Hatchwell and SH Elsea

      Version of Record online: 26 JUN 2007 | DOI: 10.1111/j.1399-0004.2007.00831.x

  4. Letters to the Editor

    1. Top of page
    2. Developmental Biology: Frontiers for Clinical Genetics
    3. HotSpots
    4. Short Reports
    5. Letters to the Editor
    1. Congenital myasthenic syndrome caused by two non-N88K rapsyn mutations (pages 63–65)

      RA Maselli, H Dris, J Schnier, JL Cockrell and RL Wollmann

      Version of Record online: 26 JUN 2007 | DOI: 10.1111/j.1399-0004.2007.00824.x

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