American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

15 March 1991

Volume 38, Issue 4

Pages fmi–fmi, 517–639

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. In Memoriam
    4. Brief Clinical Report
    5. Articles
    6. New Syndrome
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Brief Clinical Report
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Letter to the Editors
    15. Articles
    16. Letter to the Editors
    17. Articles
    1. You have free access to this content
      Masthead (page fmi)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380401

  2. In Memoriam

    1. Top of page
    2. Masthead
    3. In Memoriam
    4. Brief Clinical Report
    5. Articles
    6. New Syndrome
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Brief Clinical Report
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Letter to the Editors
    15. Articles
    16. Letter to the Editors
    17. Articles
    1. Richard M. Goodman, M.D. (page 517)

      David E. Comings

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380402

  3. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. In Memoriam
    4. Brief Clinical Report
    5. Articles
    6. New Syndrome
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Brief Clinical Report
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Letter to the Editors
    15. Articles
    16. Letter to the Editors
    17. Articles
    1. Duplication 3q(q21 [RIGHTWARDS ARROW] qter) without limb anomalies (pages 518–522)

      Suzan R. Ismail, Boris G. Kousseff, Samia M. Kotb and Soha F. Kholeif

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380403

  4. Articles

    1. Top of page
    2. Masthead
    3. In Memoriam
    4. Brief Clinical Report
    5. Articles
    6. New Syndrome
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Brief Clinical Report
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Letter to the Editors
    15. Articles
    16. Letter to the Editors
    17. Articles
  5. New Syndrome

    1. Top of page
    2. Masthead
    3. In Memoriam
    4. Brief Clinical Report
    5. Articles
    6. New Syndrome
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Brief Clinical Report
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Letter to the Editors
    15. Articles
    16. Letter to the Editors
    17. Articles
  6. Articles

    1. Top of page
    2. Masthead
    3. In Memoriam
    4. Brief Clinical Report
    5. Articles
    6. New Syndrome
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Brief Clinical Report
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Letter to the Editors
    15. Articles
    16. Letter to the Editors
    17. Articles
    1. Interstitial 15q deletion without a classic Prader-Willi phenotype (pages 532–534)

      Dr. Francisco Galán, María Soledad Aguilar, Juan González, Fernando Clemente, Rafael Sánchez, Manuel Tapia and Manuel Moya

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380406

  7. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. In Memoriam
    4. Brief Clinical Report
    5. Articles
    6. New Syndrome
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Brief Clinical Report
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Letter to the Editors
    15. Articles
    16. Letter to the Editors
    17. Articles
    1. Ectrodactyly, cleft lip/palate syndrome (pages 539–541)

      Elaine S. O. Rodini, J. A. S. Freitas and A. Richieri-Costa

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380408

  8. Articles

    1. Top of page
    2. Masthead
    3. In Memoriam
    4. Brief Clinical Report
    5. Articles
    6. New Syndrome
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Brief Clinical Report
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Letter to the Editors
    15. Articles
    16. Letter to the Editors
    17. Articles
    1. The cardio-facio-cutaneous (CFC) syndrome and Noonan syndrome: Are they the same? (pages 548–551)

      Dr. A. E. Fryer, P. J. Holt and H. E. Hughes

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320380410

    2. A distinct type of hidrotic ectodermal dysplasia (pages 552–556)

      Dr. Fahed Halal, Nora Setton and Nai-San Wang

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320380411

    3. Association of distal arthrogryposis, mental retardation, whistling face, and pierre robin sequence: Evidence for nosologic heterogeneity (pages 557–561)

      Constance Schrander-Stumpel, Jean Pierre Fryns, Frits A. Beemer and Frans A. Rive

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320380412

  9. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. In Memoriam
    4. Brief Clinical Report
    5. Articles
    6. New Syndrome
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Brief Clinical Report
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Letter to the Editors
    15. Articles
    16. Letter to the Editors
    17. Articles
    1. Floating-Harbor syndrome and celiac disease (pages 562–564)

      Dr. Albert E. Chudley and Stanley P. Moroz

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380413

  10. Articles

    1. Top of page
    2. Masthead
    3. In Memoriam
    4. Brief Clinical Report
    5. Articles
    6. New Syndrome
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Brief Clinical Report
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Letter to the Editors
    15. Articles
    16. Letter to the Editors
    17. Articles
    1. Prevalence study of Rett syndrome in North Dakota children (pages 565–568)

      Larry Burd, Barbara Vesley, John T. Martsolf and Jacob Kerbeshian

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380414

    2. Digeorge anomaly in an infant with deletion of chromosome 22 and dup(9p) due to adjacent type II disjunction (pages 569–573)

      Dr. Mohamed H. El-Fouly, James V. Higgins, Saroj Kapur, Beverly J. Sankey, David N. Matisoff and Maria Costa-Fox

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380415

    3. Variability of expression of the orofaciodigital syndrome type I in black females: Six cases (pages 574–582)

      Carlos F. Salinas, G. Shashidhar Pai, Christian L. Vera, Jovan Milutinovic, Richard Hagerty, Joel D. Cooper and David R. Cagna

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320380416

    4. Renal and skin involvement in a patient with complete Kearns-Sayre syndrome (pages 583–587)

      Dr. Kazuhiro Mori, Kouji Narahara, Shinsuke Ninomiya, Yu-ichi Goto and Ikuya Nonaka

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320380417

    5. DNA polymorphisms and deletion analysis of the Duchenne–Becker muscular dystrophy gene in the chinese (pages 593–600)

      Bing-Wen Soong, Ting-Fen Tsai, Chume-Hwae Su, Ko-Pei Kao, Kwang-Jen Hsiao and Tsung-Sheng Su

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320380419

    6. Balanced translocation 12/13 and situs abnormalities: Homology of early pattern formation in man and lower organisms? (pages 601–607)

      Golder N. Wilson, J. Patrick Stout, Nancy R. Schneider, Susan M. Zneimer and Larry C. Gilstrap

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320380420

  11. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. In Memoriam
    4. Brief Clinical Report
    5. Articles
    6. New Syndrome
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Brief Clinical Report
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Letter to the Editors
    15. Articles
    16. Letter to the Editors
    17. Articles
    1. Interstitial deletion of the long arm of chromosome 6 associated with absent pulmonary valve (pages 608–611)

      Hitoshi Horigome, Takako Takano, Takeki Hirano, Takako Kajima and Shin-Ichi Ohtani

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320380421

  12. Articles

    1. Top of page
    2. Masthead
    3. In Memoriam
    4. Brief Clinical Report
    5. Articles
    6. New Syndrome
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Brief Clinical Report
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Letter to the Editors
    15. Articles
    16. Letter to the Editors
    17. Articles
    1. Tetrasomy of the short arm of chromosome 9: Prenatal diagnosis and further delineation of the phenotype (pages 612–615)

      G. Bradley Schaefer, David B. Domek, Mark A. Morgan, Razia S. Muneer and Sarah F. Johnson

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320380422

    2. Epidemiological aspects of Mendelian syndromes in a spanish population sample: I. Autosomal dominant malformation syndromes (pages 622–625)

      M. L. Martínez-Frías, A. Cereijo, E. Bermejo, M. López, M. Sánchez and C. Gonzalo

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380424

    3. Epidemiological aspects of Mendelian syndromes in a Spanish population sample: II. Autosomal recessive malformation syndromes (pages 626–629)

      M. L. Martínez-Frías, E. Bermejo, A. Cereijo, M. Sánchez, M. López and C. Gonzalo

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320380425

  13. Letter to the Editors

    1. Top of page
    2. Masthead
    3. In Memoriam
    4. Brief Clinical Report
    5. Articles
    6. New Syndrome
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Brief Clinical Report
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Letter to the Editors
    15. Articles
    16. Letter to the Editors
    17. Articles
  14. Articles

    1. Top of page
    2. Masthead
    3. In Memoriam
    4. Brief Clinical Report
    5. Articles
    6. New Syndrome
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Brief Clinical Report
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Letter to the Editors
    15. Articles
    16. Letter to the Editors
    17. Articles
    1. Reply to Dr. Gericke (page 632)

      N. G. Hartwig, Chr. Vermeij-Keers and J. A. Bruijn

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320380427

  15. Letter to the Editors

    1. Top of page
    2. Masthead
    3. In Memoriam
    4. Brief Clinical Report
    5. Articles
    6. New Syndrome
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Brief Clinical Report
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Letter to the Editors
    15. Articles
    16. Letter to the Editors
    17. Articles
    1. Rejoinder by Dr. Gericke to Dr. Hartwig and Coworkers (page 633)

      Prof. G. S. Gericke, E. J. Van Rensburg, D. Mitchell, H. Laburn and H. Isaacs

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320380428

  16. Articles

    1. Top of page
    2. Masthead
    3. In Memoriam
    4. Brief Clinical Report
    5. Articles
    6. New Syndrome
    7. Articles
    8. Brief Clinical Report
    9. Articles
    10. Brief Clinical Report
    11. Articles
    12. Brief Clinical Report
    13. Articles
    14. Letter to the Editors
    15. Articles
    16. Letter to the Editors
    17. Articles

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