American Journal of Medical Genetics Part A

Cover image for American Journal of Medical Genetics Part A

1 May 2004

Volume 126A, Issue 4

Pages 331–439

  1. Invited Comment

    1. Top of page
    2. Invited Comment
    3. Research Articles
    4. Research Reviews
    5. Research Review
    6. Research Reviews
    7. Research Articles
    8. Clinical Reports
    9. Research Letters
    10. Book Reviews
    11. Correspondence
    1. The challenge in hidden treasures: A never ending story (pages 331–332)

      Dr. Raoul C.M. Hennekam

      Version of Record online: 30 MAR 2004 | DOI: 10.1002/ajmg.a.20659

  2. Research Articles

    1. Top of page
    2. Invited Comment
    3. Research Articles
    4. Research Reviews
    5. Research Review
    6. Research Reviews
    7. Research Articles
    8. Clinical Reports
    9. Research Letters
    10. Book Reviews
    11. Correspondence
    1. Peroxisome biogenesis disorders with prolonged survival: Phenotypic expression in a cohort of 31 patients (pages 333–338)

      Bwee Tien Poll-The, Jeannette Gootjes, Marinus Duran, Johannis B.C. de Klerk, Liesbeth J. Maillette de Buy Wenniger-Prick, Ronald J.C. Admiraal, Hans R. Waterham, Ronald J.A. Wanders and Peter G. Barth

      Version of Record online: 30 MAR 2004 | DOI: 10.1002/ajmg.a.20664

    2. 3D analysis of facial morphology (pages 339–348)

      Peter Hammond, Tim J. Hutton, Judith E. Allanson, Linda E. Campbell, Raoul C.M. Hennekam, Sean Holden, Michael A. Patton, Adam Shaw, I. Karen Temple, Matthew Trotter, Kieran C. Murphy and Robin M. Winter

      Version of Record online: 14 APR 2004 | DOI: 10.1002/ajmg.a.20665

  3. Research Reviews

    1. Top of page
    2. Invited Comment
    3. Research Articles
    4. Research Reviews
    5. Research Review
    6. Research Reviews
    7. Research Articles
    8. Clinical Reports
    9. Research Letters
    10. Book Reviews
    11. Correspondence
    1. X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): An update (pages 349–354)

      Peter G. Barth, Fredoen Valianpour, Valerie M. Bowen, Jan Lam, Marinus Duran, Frédéric M. Vaz and Ronald J.A. Wanders

      Version of Record online: 27 JAN 2004 | DOI: 10.1002/ajmg.a.20660

  4. Research Review

    1. Top of page
    2. Invited Comment
    3. Research Articles
    4. Research Reviews
    5. Research Review
    6. Research Reviews
    7. Research Articles
    8. Clinical Reports
    9. Research Letters
    10. Book Reviews
    11. Correspondence
  5. Research Reviews

    1. Top of page
    2. Invited Comment
    3. Research Articles
    4. Research Reviews
    5. Research Review
    6. Research Reviews
    7. Research Articles
    8. Clinical Reports
    9. Research Letters
    10. Book Reviews
    11. Correspondence
  6. Research Articles

    1. Top of page
    2. Invited Comment
    3. Research Articles
    4. Research Reviews
    5. Research Review
    6. Research Reviews
    7. Research Articles
    8. Clinical Reports
    9. Research Letters
    10. Book Reviews
    11. Correspondence
    1. Duplication of the distal long arm of chromosome 15: Report of three new patients and review of the literature (pages 398–402)

      Jennifer A. Roggenbuck, Nancy J. Mendelsohn, Beverly Tenenholz, Roger L. Ladda and James M. Fink

      Version of Record online: 26 NOV 2003 | DOI: 10.1002/ajmg.a.20617

    2. Does autosomal dominant pseudoxanthoma elasticum exist? (pages 403–412)

      Astrid S. Plomp, Xiaofeng Hu, Paulus T.V.M. de Jong and Arthur A.B. Bergen

      Version of Record online: 26 NOV 2003 | DOI: 10.1002/ajmg.a.20632

  7. Clinical Reports

    1. Top of page
    2. Invited Comment
    3. Research Articles
    4. Research Reviews
    5. Research Review
    6. Research Reviews
    7. Research Articles
    8. Clinical Reports
    9. Research Letters
    10. Book Reviews
    11. Correspondence
    1. Prenatal diagnosis of a rare inherited heterochromatic variant chromosome 4 (pages 420–422)

      Ann-Leslie Zaslav, Guy Pierno, Arthur Fougner, Jessy Jacob, Geraldine Shikora, Rehana Kazi, Donna Blumenthal, Fakhry Alexander and Joyce E. Fox

      Version of Record online: 26 NOV 2003 | DOI: 10.1002/ajmg.a.20594

    2. Familial interstitial duplication of 11q; partial trisomy (11)(q13.5q21) (pages 423–426)

      Krishna K. Yelavarthi and Janice Zunich

      Version of Record online: 26 NOV 2003 | DOI: 10.1002/ajmg.a.20610

    3. Two new cases of Barraquer–Simons syndrome (pages 427–429)

      A. Ferrarini, D. Milani, M. Bottigelli, G. Cagnoli and Angelo Selicorni

      Version of Record online: 26 NOV 2003 | DOI: 10.1002/ajmg.a.20623

  8. Research Letters

    1. Top of page
    2. Invited Comment
    3. Research Articles
    4. Research Reviews
    5. Research Review
    6. Research Reviews
    7. Research Articles
    8. Clinical Reports
    9. Research Letters
    10. Book Reviews
    11. Correspondence
    1. Frequency of neural tube defects and down syndrome in the same sibship: Analysis of the Spanish ongoing case-control study (pages 430–431)

      María Luisa Martínez-Frías, Laura Rodríguez, Fermina López-Grondona, Eva Bermejo, Elvira Rodríguez-Pinilla and Jaime L. Frías

      Version of Record online: 26 NOV 2003 | DOI: 10.1002/ajmg.a.20635

  9. Book Reviews

    1. Top of page
    2. Invited Comment
    3. Research Articles
    4. Research Reviews
    5. Research Review
    6. Research Reviews
    7. Research Articles
    8. Clinical Reports
    9. Research Letters
    10. Book Reviews
    11. Correspondence
    1. Catalogue of unbalanced chromosome aberrations in man (pages 435–436)

      Dorothy Warburton

      Version of Record online: 26 NOV 2003 | DOI: 10.1002/ajmg.a.20641

  10. Correspondence

    1. Top of page
    2. Invited Comment
    3. Research Articles
    4. Research Reviews
    5. Research Review
    6. Research Reviews
    7. Research Articles
    8. Clinical Reports
    9. Research Letters
    10. Book Reviews
    11. Correspondence
    1. Response to Kessler and Resta's commentary (page 439)

      Nathaniel H. Robin

      Version of Record online: 21 OCT 2003 | DOI: 10.1002/ajmg.a.20567

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