Clinical Genetics

Cover image for Clinical Genetics

April 2007

Volume 71, Issue 4

Pages 295–377

  1. Developmental Biology: Frontiers for Clinical Genetics

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

    1. Top of page
    2. Developmental Biology: Frontiers for Clinical Genetics
    3. Original Articles
    4. Short Reports
    5. Letters to the Editor
    1. Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations (pages 311–319)

      YP Goldberg, J MacFarlane, ML MacDonald, J Thompson, M-P Dube, M Mattice, R Fraser, C Young, S Hossain, T Pape, B Payne, C Radomski, G Donaldson, E Ives, J Cox, HB Younghusband, R Green, A Duff, E Boltshauser, GA Grinspan, JH Dimon, BG Sibley, G Andria, E Toscano, J Kerdraon, D Bowsher, SN Pimstone, ME Samuels, R Sherrington and MR Hayden

      Article first published online: 26 MAR 2007 | DOI: 10.1111/j.1399-0004.2007.00790.x

  3. Short Reports

    1. Top of page
    2. Developmental Biology: Frontiers for Clinical Genetics
    3. Original Articles
    4. Short Reports
    5. Letters to the Editor
    1. The p.R1109X mutation in SH3TC2 gene is predominant in Spanish Gypsies with Charcot–Marie–Tooth disease type 4 (pages 343–349)

      R Claramunt, T Sevilla, V Lupo, A Cuesta, JM Millán, JJ Vílchez, F Palau and C Espinós

      Article first published online: 25 APR 2007 | DOI: 10.1111/j.1399-0004.2007.00774.x

    2. A novel homozygous frameshift deletion c.471del of HFE associated with hemochromatosis (pages 350–353)

      M Cukjati, S Koren, V Čurin Šerbec, B Vidan-Jeras and R Rupreht

      Article first published online: 25 APR 2007 | DOI: 10.1111/j.1399-0004.2007.00777.x

    3. Should NF2 mutation screening be undertaken in patients with an apparently isolated vestibular schwannoma? (pages 354–358)

      DGR Evans, RT Ramsden, C Gokhale, N Bowers, SM Huson and A Wallace

      Article first published online: 25 APR 2007 | DOI: 10.1111/j.1399-0004.2007.00778.x

    4. Association of TCF7L2 polymorphisms with type 2 diabetes in Mexico City (pages 359–366)

      EJ Parra, E Cameron, L Simmonds, A Valladares, P McKeigue, M Shriver, N Wacher, J Kumate, R Kittles and M Cruz

      Article first published online: 25 APR 2007 | DOI: 10.1111/j.1399-0004.2007.00780.x

  4. Letters to the Editor

    1. Top of page
    2. Developmental Biology: Frontiers for Clinical Genetics
    3. Original Articles
    4. Short Reports
    5. Letters to the Editor
    1. LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson’s disease (pages 367–370)

      D Civitelli, P Tarantino, G Nicoletti, IC Cirò Candiano, F Annesi, EV De Marco, S Carrideo, FE Rocca, F Condino, P Spadafora, P Pugliese, S D’Asero, M Morelli, S Paglionico, G Annesi and A Quattrone

      Article first published online: 25 APR 2007 | DOI: 10.1111/j.1399-0004.2007.00771.x

    2. Tuberous sclerosis complex and myocardial fat-containing lesions: a report of four cases (pages 371–373)

      EB Winterkorn, JD Dodd, I Inglessis, G Holmvang and EA Thiele

      Article first published online: 25 APR 2007 | DOI: 10.1111/j.1399-0004.2007.00775.x

    3. Late-onset GSDII with novel GAA gene mutation (pages 374–375)

      C Angelini and AC Nascimbeni

      Article first published online: 25 APR 2007 | DOI: 10.1111/j.1399-0004.2007.00785.x

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