American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

1 March 1994

Volume 50, Issue 1

Pages fmi–fmi, 1–103, i–i

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Letters to the Editor
    7. Reply
    8. Articles
    9. Letters to the Editor
    10. Book Review
    11. Announcement
    1. Masthead (page fmi)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320500101

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Letters to the Editor
    7. Reply
    8. Articles
    9. Letters to the Editor
    10. Book Review
    11. Announcement
    1. Attitudes of physicians and genetics professionals toward cystic fibrosis carrier screening (pages 1–11)

      Ruth R. Faden, Ellen S. Tambor, Gary A. Chase, Gail Geller, Karen J. Hofman and Neil A. Holtzman

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320500102

    2. Prenatal diagnosis of unusual hemoglobinopathies (pages 15–20)

      Jong-Hwa Kim, Roger V. Lebo, Shi-Ping Cai, Xia Su, Jae-Hyun Chung, William C. Mentzer and Mitchell S. Golbus

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320500104

    3. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization (pages 21–27)

      B. R. DuPont, R. W. Huff, L. E. Ridgway, R. F. Stratton and C. M. Moore

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320500105

  3. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Letters to the Editor
    7. Reply
    8. Articles
    9. Letters to the Editor
    10. Book Review
    11. Announcement
    1. Confirmation of proximal 1q duplication using fluorescence in situ hybridization (pages 28–31)

      Harold Chen, Christine J. Kusyk, Cathy M. Tuck-Muller, Jose E. Martinez, Rodney D. Dorand and Wladimir Wertelecki

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320500106

  4. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Letters to the Editor
    7. Reply
    8. Articles
    9. Letters to the Editor
    10. Book Review
    11. Announcement
    1. Clinical diagnosis of the Usher syndromes (pages 32–38)

      R. J. H. Smith, C. I. Berlin, J. F. Hejtmancik, B. J. B. Keats, W. J. Kimberling, R. A. Lewis, C. G. Möller, M. Z. Pelias and L. Tranebjærǵ

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320500107

  5. Letters to the Editor

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Letters to the Editor
    7. Reply
    8. Articles
    9. Letters to the Editor
    10. Book Review
    11. Announcement
  6. Reply

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Letters to the Editor
    7. Reply
    8. Articles
    9. Letters to the Editor
    10. Book Review
    11. Announcement
  7. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Letters to the Editor
    7. Reply
    8. Articles
    9. Letters to the Editor
    10. Book Review
    11. Announcement
    1. Hypoplasia of the cerebellar vermis and corpus callosum in thrombocytopenia with absent radius syndrome on MRI studies (pages 46–50)

      Madeleine R. MacDonald, G. Bradley Schaefer, Ann Haskins Olney and Donna F. Patton

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320500111

    2. Confined placental chimerism: Prenatal and postnatal cytogenetic and molecular analysis, and pregnancy outcome (pages 51–56)

      Tziporah C. Falik-Borenstein, Julie R. Korenberg and Rhona R. Schreck

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320500112

    3. Isochromosome 15q of maternal origin in two Prader-Willi syndrome patients previously diagnosed erroneously as cytogenetic deletions (pages 64–67)

      Shinji Saitoh, Apiwat Mutirangura, Akira Kuwano, David H. Ledbetter and Norio Niikawa

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320500114

    4. Heteroduplex analysis of the dystrophin gene: Application to point mutation and carrier detection (pages 68–73)

      Thomas W. Prior, Audrey C. Papp, Pamela J. Snyder, Mary S. Sedra, Lorraine M. Western, Claire Bartolo, Richard T. Moxley and Jerry R. Mendell

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320500115

    5. Ataxia, mental deterioration, epilepsy in a family with dominant enamel hypoplasia: A variant of Kohlschütter-Tönz syndrome? (pages 79–83)

      Giancarlo Guazzi, Dr. Silvia Palmeri, Alessandro Malandrini, Giuseppe Ciacci, Raoul Di Perri, Grazia Mancini, Corrado Messina and Claudio Salvadori

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320500117

    6. Occurrence of two different intragenic deletions in two male relatives affected with Duchenne muscular dystrophy (pages 84–86)

      M. L. Mostacciuolo, M. Miorin, L. Vitiello, A. Rampazzo, M. Fanin, C. Angelini and G. A. Danieli

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320500118

    7. Congenital hypoplastic anemia: Another example of autosomal dominant transmission (pages 87–89)

      V. Gojic, E. T. Van't Veer-Korthof, L. J. Bosch, W. H. Puyn and A. van Haeringen

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320500119

    8. Three new cases of the Schinzel-Giedion syndrome and review of the literature (pages 90–93)

      Philippe Labrune, Stanislas Lyonnet, Véronique Zupan, Marie-Claire Imbert, Françoise Goutieres, Philippe Hubert and Martine Le Merrer

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320500120

  8. Letters to the Editor

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Letters to the Editor
    7. Reply
    8. Articles
    9. Letters to the Editor
    10. Book Review
    11. Announcement
    1. Renal tubular dysgenesis (pages 96–97)

      Dr. Kamal Akl and Bahram Azadeh

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320500122

    2. Fanconi anemia in a child previously diagnosed as Baller-Gerold syndrome (pages 98–99)

      Dr. S. A. Farrell, Bosco A. Paes and M. E. Suzanne Lewis

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320500123

    3. Hereditary nodular heterotopia accompanied by mega cisterna magna (page 100)

      Dr. Francis J. DiMario Jr., Richard J. Cobb, Gale R. Ramsby and Carol Leicher

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320500124

    4. Genes for split hand/split foot and laterality defects on 7q22.1 and xq24-q27.1 (page 101)

      Dr. Maurizio Genuardi, Fiorella Gurrieri and Giovanni Neri

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320500125

  9. Book Review

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Letters to the Editor
    7. Reply
    8. Articles
    9. Letters to the Editor
    10. Book Review
    11. Announcement
  10. Announcement

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Letters to the Editor
    7. Reply
    8. Articles
    9. Letters to the Editor
    10. Book Review
    11. Announcement
    1. You have free access to this content
      Announcement (page i)

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320500127

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