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Clinical Genetics

Cover image for Clinical Genetics

August 2013

Volume 84, Issue 2

Pages 99–199

  1. PERSPECTIVES

    1. Top of page
    2. PERSPECTIVES
    3. REVIEWS
    4. SHORT REPORT
    5. REVIEWS
    6. NOVEL GENE DISCOVERIES
    7. REVIEWS
    8. ORIGINAL ARTICLES
    9. REVIEWS
    10. ORIGINAL ARTICLES
    11. LETTER TO THE EDITOR
    1. You have free access to this content
  2. REVIEWS

    1. Top of page
    2. PERSPECTIVES
    3. REVIEWS
    4. SHORT REPORT
    5. REVIEWS
    6. NOVEL GENE DISCOVERIES
    7. REVIEWS
    8. ORIGINAL ARTICLES
    9. REVIEWS
    10. ORIGINAL ARTICLES
    11. LETTER TO THE EDITOR
    1. You have free access to this content
    2. You have free access to this content
    3. You have free access to this content
  3. SHORT REPORT

    1. Top of page
    2. PERSPECTIVES
    3. REVIEWS
    4. SHORT REPORT
    5. REVIEWS
    6. NOVEL GENE DISCOVERIES
    7. REVIEWS
    8. ORIGINAL ARTICLES
    9. REVIEWS
    10. ORIGINAL ARTICLES
    11. LETTER TO THE EDITOR
    1. You have free access to this content
      Mutations in ALDH1A3 cause microphthalmia (pages 128–131)

      M A Aldahmesh, A O Khan, H Hijazi and F S Alkuraya

      Article first published online: 27 MAY 2013 | DOI: 10.1111/cge.12184

  4. REVIEWS

    1. Top of page
    2. PERSPECTIVES
    3. REVIEWS
    4. SHORT REPORT
    5. REVIEWS
    6. NOVEL GENE DISCOVERIES
    7. REVIEWS
    8. ORIGINAL ARTICLES
    9. REVIEWS
    10. ORIGINAL ARTICLES
    11. LETTER TO THE EDITOR
    1. You have free access to this content
      Genes and mutations causing retinitis pigmentosa (pages 132–141)

      S P Daiger, L S Sullivan and S J Bowne

      Article first published online: 19 JUN 2013 | DOI: 10.1111/cge.12203

    2. You have free access to this content
  5. NOVEL GENE DISCOVERIES

    1. Top of page
    2. PERSPECTIVES
    3. REVIEWS
    4. SHORT REPORT
    5. REVIEWS
    6. NOVEL GENE DISCOVERIES
    7. REVIEWS
    8. ORIGINAL ARTICLES
    9. REVIEWS
    10. ORIGINAL ARTICLES
    11. LETTER TO THE EDITOR
    1. You have full text access to this OnlineOpen article
      WDR19: An ancient, retrograde, intraflagellar ciliary protein is mutated in autosomal recessive retinitis pigmentosa and in Senior-Loken syndrome (pages 150–159)

      R G Coussa, E A Otto, H-Y Gee, P Arthurs, H Ren, I Lopez, V Keser, Q Fu, R Faingold, A Khan, J Schwartzentruber, J Majewski, F Hildebrandt and R K Koenekoop

      Article first published online: 9 JUL 2013 | DOI: 10.1111/cge.12196

  6. REVIEWS

    1. Top of page
    2. PERSPECTIVES
    3. REVIEWS
    4. SHORT REPORT
    5. REVIEWS
    6. NOVEL GENE DISCOVERIES
    7. REVIEWS
    8. ORIGINAL ARTICLES
    9. REVIEWS
    10. ORIGINAL ARTICLES
    11. LETTER TO THE EDITOR
    1. You have full text access to this OnlineOpen article
  7. ORIGINAL ARTICLES

    1. Top of page
    2. PERSPECTIVES
    3. REVIEWS
    4. SHORT REPORT
    5. REVIEWS
    6. NOVEL GENE DISCOVERIES
    7. REVIEWS
    8. ORIGINAL ARTICLES
    9. REVIEWS
    10. ORIGINAL ARTICLES
    11. LETTER TO THE EDITOR
    1. You have full text access to this OnlineOpen article
      Variations in COL15A1 and COL18A1 influence age of onset of primary open angle glaucoma (pages 167–174)

      J L Wiggs, G R Howell, K Linkroum, W Abdrabou, E Hodges, C E Braine, L R Pasquale, G J Hannon, J L Haines and S W M John

      Article first published online: 27 MAY 2013 | DOI: 10.1111/cge.12176

    2. You have free access to this content
  8. REVIEWS

    1. Top of page
    2. PERSPECTIVES
    3. REVIEWS
    4. SHORT REPORT
    5. REVIEWS
    6. NOVEL GENE DISCOVERIES
    7. REVIEWS
    8. ORIGINAL ARTICLES
    9. REVIEWS
    10. ORIGINAL ARTICLES
    11. LETTER TO THE EDITOR
    1. You have free access to this content
  9. ORIGINAL ARTICLES

    1. Top of page
    2. PERSPECTIVES
    3. REVIEWS
    4. SHORT REPORT
    5. REVIEWS
    6. NOVEL GENE DISCOVERIES
    7. REVIEWS
    8. ORIGINAL ARTICLES
    9. REVIEWS
    10. ORIGINAL ARTICLES
    11. LETTER TO THE EDITOR
    1. You have free access to this content
  10. LETTER TO THE EDITOR

    1. Top of page
    2. PERSPECTIVES
    3. REVIEWS
    4. SHORT REPORT
    5. REVIEWS
    6. NOVEL GENE DISCOVERIES
    7. REVIEWS
    8. ORIGINAL ARTICLES
    9. REVIEWS
    10. ORIGINAL ARTICLES
    11. LETTER TO THE EDITOR
    1. You have free access to this content
      Homozygous truncation of SIX6 causes complex microphthalmia in humans (pages 198–199)

      M A Aldahmesh, A O Khan, H Hijazi and F S Alkuraya

      Article first published online: 20 NOV 2012 | DOI: 10.1111/cge.12046

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