Clinical Genetics

Cover image for Clinical Genetics

August 2005

Volume 68, Issue 2

Pages 97–191

  1. Mini Review

    1. Top of page
    2. Mini Review
    3. Developmental Biology
    4. HotSpots
    5. Original Articles
    6. Short Reports
    7. Letters to the Editor
  2. Developmental Biology

    1. Top of page
    2. Mini Review
    3. Developmental Biology
    4. HotSpots
    5. Original Articles
    6. Short Reports
    7. Letters to the Editor
  3. HotSpots

    1. Top of page
    2. Mini Review
    3. Developmental Biology
    4. HotSpots
    5. Original Articles
    6. Short Reports
    7. Letters to the Editor
  4. Original Articles

    1. Top of page
    2. Mini Review
    3. Developmental Biology
    4. HotSpots
    5. Original Articles
    6. Short Reports
    7. Letters to the Editor
    1. Rare SP-A alleles and the SP-A1-6A4 allele associate with risk for lung carcinoma (pages 128–136)

      C Seifart, H-M Lin, U Seifart, A Plagens, S DiAngelo, P Von Wichert and J Floros

      Version of Record online: 17 JUN 2005 | DOI: 10.1111/j.1399-0004.2005.00470.x

    2. Clinical and molecular characteristics of hereditary non-polyposis colorectal cancer families in Southeast Asia (pages 137–145)

      S-C Lee, J-Y Guo, R Lim, R Soo, E Koay, M Salto-Tellez, A Leong and B-C Goh

      Version of Record online: 23 MAY 2005 | DOI: 10.1111/j.1399-0004.2005.00469.x

  5. Short Reports

    1. Top of page
    2. Mini Review
    3. Developmental Biology
    4. HotSpots
    5. Original Articles
    6. Short Reports
    7. Letters to the Editor
    1. Functional analysis of R75Q mutation in the gene coding for Connexin 26 identified in a family with nonsyndromic hearing loss (pages 161–166)

      V Piazza, M Beltramello, M Menniti, E Colao, P Malatesta, R Argento, G Chiarella, LV Gallo, M Catalano, N Perrotti, F Mammano and E Cassandro

      Version of Record online: 17 JUN 2005 | DOI: 10.1111/j.1399-0004.2005.00468.x

    2. Two novel CLN6 mutations in variant late-infantile neuronal ceroid lipofuscinosis patients of Turkish origin (pages 167–173)

      E Siintola, M Topcu, A Kohlschütter, T Salonen, T Joensuu, A-K Anttonen and A-E Lehesjoki

      Version of Record online: 17 JUN 2005 | DOI: 10.1111/j.1399-0004.2005.00471.x

  6. Letters to the Editor

    1. Top of page
    2. Mini Review
    3. Developmental Biology
    4. HotSpots
    5. Original Articles
    6. Short Reports
    7. Letters to the Editor

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