Clinical Genetics

Cover image for Clinical Genetics

June 2003

Volume 63, Issue 6

Pages 1–555

  1. Author and keyword Index

    1. Top of page
    2. Author and keyword Index
    3. Review Article
    4. Developmental Biology: Frontiers for Clinical Genetics
    5. Hotspots
    6. Original Articles
    7. Short Reports
    8. Letter to the Editor
    9. Volume Index 63
    1. Subject index (pages 1–6)

      Version of Record online: 25 AUG 2009 | DOI: 10.1111/j.1399-0004.2003.sindex.x

    2. Author index (pages 1–2)

      Version of Record online: 25 AUG 2009 | DOI: 10.1111/j.1399-0004.2003.aindex.x

  2. Review Article

    1. Top of page
    2. Author and keyword Index
    3. Review Article
    4. Developmental Biology: Frontiers for Clinical Genetics
    5. Hotspots
    6. Original Articles
    7. Short Reports
    8. Letter to the Editor
    9. Volume Index 63
    1. The molecular genetics of Usher syndrome (pages 431–444)

      ZM Ahmed, S Riazuddin, S Riazuddin and ER Wilcox

      Version of Record online: 3 JUN 2003 | DOI: 10.1034/j.1399-0004.2003.00109.x

  3. Developmental Biology: Frontiers for Clinical Genetics

    1. Top of page
    2. Author and keyword Index
    3. Review Article
    4. Developmental Biology: Frontiers for Clinical Genetics
    5. Hotspots
    6. Original Articles
    7. Short Reports
    8. Letter to the Editor
    9. Volume Index 63
  4. Hotspots

    1. Top of page
    2. Author and keyword Index
    3. Review Article
    4. Developmental Biology: Frontiers for Clinical Genetics
    5. Hotspots
    6. Original Articles
    7. Short Reports
    8. Letter to the Editor
    9. Volume Index 63
    1. Ankyrin-B mutations in familial cardiac arrhythmia (pages 458–459)

      B J Haigh

      Version of Record online: 3 JUN 2003 | DOI: 10.1034/j.1399-0004.2003.t01-1-00095.x

  5. Original Articles

    1. Top of page
    2. Author and keyword Index
    3. Review Article
    4. Developmental Biology: Frontiers for Clinical Genetics
    5. Hotspots
    6. Original Articles
    7. Short Reports
    8. Letter to the Editor
    9. Volume Index 63
    1. Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000 (pages 462–475)

      S Creighton, EW Almqvist, D MacGregor, B Fernandez, H Hogg, J Beis, JP Welch, C Riddell, R Lokkesmoe, M Khalifa, J MacKenzie, A Sajoo, S Farrell, F Robert, A Shugar, A Summers, W Meschino, D Allingham-Hawkins, T Chiu, A Hunter, J Allanson, H Hare, J Schween, L Collins, S Sanders, C Greenberg, S Cardwell, E Lemire, P MacLeod and MR Hayden

      Version of Record online: 3 JUN 2003 | DOI: 10.1034/j.1399-0004.2003.00093.x

    2. Analysis of splice-site mutations of the α-galactosidase A gene in Fabry disease (pages 476–482)

      L-W Lai, O Whitehair, M-J Wu, M O'Meara and Y-HH Lien

      Version of Record online: 3 JUN 2003 | DOI: 10.1034/j.1399-0004.2003.00077.x

    3. Intact fetal cell isolation from maternal blood: improved isolation using a simple whole blood progenitor cell enrichment approach (RosetteSep) (pages 483–489)

      FZ Bischoff, DA Marquéz-Do, DI Martinez, D Dang, C Horne, D Lewis and JL Simpson

      Version of Record online: 3 JUN 2003 | DOI: 10.1034/j.1399-0004.2003.00087.x

    4. Neurological presentation of Ehlers–Danlos syndrome type IV in a family with parental mosaicism (pages 510–515)

      S Palmeri, F Mari, I Meloni, A Malandrini, F Ariani, M Villanova, A Pompilio, U Schwarze, PH Byers and A Renieri

      Version of Record online: 3 JUN 2003 | DOI: 10.1034/j.1399-0004.2003.00075.x

  6. Short Reports

    1. Top of page
    2. Author and keyword Index
    3. Review Article
    4. Developmental Biology: Frontiers for Clinical Genetics
    5. Hotspots
    6. Original Articles
    7. Short Reports
    8. Letter to the Editor
    9. Volume Index 63
    1. A novel dominant missense mutation – D179N – in the GJB2 gene (Connexin 26) associated with non-syndromic hearing loss (pages 516–521)

      P Primignani, P Castorina, F Sironi, C Curcio, U Ambrosetti and DA Coviello

      Version of Record online: 3 JUN 2003 | DOI: 10.1034/j.1399-0004.2003.00079.x

    2. Mapping a gene for 46,XY gonadal dysgenesis by linkage analysis (pages 530–535)

      D Jawaheer, S-HH Juo, C Le Caignec, A David, C Petit, P Gregersen, S Dowbak, A Damle, K McElreavey and H Ostrer

      Version of Record online: 3 JUN 2003 | DOI: 10.1034/j.1399-0004.2003.00082.x

    3. Endoglin gene mutations and polymorphisms in Italian patients with hereditary haemorrhagic telangiectasia (pages 536–540)

      P Lastella, C Sabbà, GM Lenato, N Resta, W Lattanzi, M Gallitelli, A Cirulli and G Guanti

      Version of Record online: 3 JUN 2003 | DOI: 10.1034/j.1399-0004.2003.00081.x

  7. Letter to the Editor

    1. Top of page
    2. Author and keyword Index
    3. Review Article
    4. Developmental Biology: Frontiers for Clinical Genetics
    5. Hotspots
    6. Original Articles
    7. Short Reports
    8. Letter to the Editor
    9. Volume Index 63
  8. Volume Index 63

    1. Top of page
    2. Author and keyword Index
    3. Review Article
    4. Developmental Biology: Frontiers for Clinical Genetics
    5. Hotspots
    6. Original Articles
    7. Short Reports
    8. Letter to the Editor
    9. Volume Index 63
    1. Author, Subject and Volume Indices (pages 543–555)

      Version of Record online: 3 JUN 2003 | DOI: 10.1034/j.1399-0004.2003.00110.x

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