Clinical Genetics

Cover image for Clinical Genetics

December 2006

Volume 70, Issue 6

Pages 457–540, i–v

  1. HotSpots

    1. Top of page
    2. HotSpots
    3. Original Article
    4. Short Reports
    5. Letters to the Editor
    6. Volume Index 70
    1. Pejvakin echoes hope for the end of silence (pages 459–460)

      JM Karasinska

      Article first published online: 10 NOV 2006 | DOI: 10.1111/j.1399-0004.2006.00709_2.x

  2. Original Article

    1. Top of page
    2. HotSpots
    3. Original Article
    4. Short Reports
    5. Letters to the Editor
    6. Volume Index 70
  3. Short Reports

    1. Top of page
    2. HotSpots
    3. Original Article
    4. Short Reports
    5. Letters to the Editor
    6. Volume Index 70
    1. Wilms’ tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism (pages 473–479)

      RH Hämäläinen, D Mowat, MT Gabbett, TA O’Brien, J Kallijärvi and A-E Lehesjoki

      Article first published online: 9 OCT 2006 | DOI: 10.1111/j.1399-0004.2006.00700.x

    2. Spastin gene mutations in Bulgarian patients with hereditary spastic paraplegia (pages 490–495)

      N Ivanova, A Löfgren, I Tournev, R Rousev, A Andreeva, A Jordanova, V Georgieva, T Deconinck, V Timmerman, I Kremensky, P De Jonghe and V Mitev

      Article first published online: 9 OCT 2006 | DOI: 10.1111/j.1399-0004.2006.00705.x

    3. Mutation analysis of BRCA1 and BRCA2 from 793 Korean patients with sporadic breast cancer (pages 496–501)

      S-H Han, K-R Lee, D-G Lee, B-Y Kim, K-E Lee and W-S Chung

      Article first published online: 10 NOV 2006 | DOI: 10.1111/j.1399-0004.2006.00717.x

    4. PKD2 gene mutation analysis in Korean autosomal dominant polycystic kidney disease patients using two-dimensional gene scanning (pages 502–508)

      W Chung, H Kim, YH Hwang, SY Kim, A-r Ko, H Ro, KB Lee, JS Lee, K-H Oh and C Ahn

      Article first published online: 10 NOV 2006 | DOI: 10.1111/j.1399-0004.2006.00721.x

      Corrected by:

      Corrigendum

      Vol. 71, Issue 2, 193, Article first published online: 23 JAN 2007

    5. Mutations in the RSK2(RPS6KA3) gene cause Coffin–Lowry syndrome and nonsyndromic X-linked mental retardation (pages 509–515)

      M Field, P Tarpey, J Boyle, S Edkins, J Goodship, Y Luo, J Moon, J Teague, MR Stratton, PA Futreal, R Wooster, FL Raymond and G Turner

      Article first published online: 10 NOV 2006 | DOI: 10.1111/j.1399-0004.2006.00723.x

    6. Clinical and molecular analysis of X-linked Charcot-Marie-Tooth disease type 1 in Spanish population (pages 516–523)

      C Casasnovas, I Banchs, J Corral, JA Martínez-Matos and V Volpini

      Article first published online: 10 NOV 2006 | DOI: 10.1111/j.1399-0004.2006.00724.x

      Corrected by:

      Corrigendum

      Vol. 73, Issue 2, 196, Article first published online: 10 JAN 2008

      Corrected by:

      Corrigendum

      Vol. 71, Issue 2, 194, Article first published online: 23 JAN 2007

  4. Letters to the Editor

    1. Top of page
    2. HotSpots
    3. Original Article
    4. Short Reports
    5. Letters to the Editor
    6. Volume Index 70
    1. Evidence against a major genetic basis for combined breast and colorectal cancer susceptibility (pages 526–529)

      H Brinkman, J Barwell, S Rose, L Tinworth, N Sodha, C Langman, L Brooks, S Payne, S Fisher, A Rowan, I Tomlinson and S Hodgson

      Article first published online: 17 OCT 2006 | DOI: 10.1111/j.1399-0004.2006.00711.x

    2. A patient with classic Rett syndrome with a novel mutation in MECP2 exon 1 (pages 530–531)

      Y Chunshu, K Endoh, M Soutome, R Kawamura and T Kubota

      Article first published online: 17 OCT 2006 | DOI: 10.1111/j.1399-0004.2006.00712.x

    3. Detection of an unusual 17p13.3 microdeletion by array comparative genomic hybridisation in a patient with lissencephaly (pages 535–537)

      E Chabchoub, T De Ravel, R Thoelen, JR Vermeesch, J-P Fryns and H Van Esch

      Article first published online: 10 NOV 2006 | DOI: 10.1111/j.1399-0004.2006.00718.x

    4. Brachydactyly type B1: report of a family with de novo ROR2 mutation (pages 538–540)

      H Hamamy, N Saleh, M Oldridge, A Al-Hadidy and K Ajlouni

      Article first published online: 10 NOV 2006 | DOI: 10.1111/j.1399-0004.2006.00719.x

  5. Volume Index 70

    1. Top of page
    2. HotSpots
    3. Original Article
    4. Short Reports
    5. Letters to the Editor
    6. Volume Index 70
    1. Author index (pages i–iii)

      Article first published online: 10 NOV 2006 | DOI: 10.1111/j.1399-0004.2006.00737.x

    2. Subject index (pages iv–v)

      Article first published online: 10 NOV 2006 | DOI: 10.1111/j.1399-0004.2006.00738.x

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