American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

December 1990

Volume 37, Issue 4

Pages fmi–fmi, 443–602

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    17. Brief Clinical Reports
    18. Articles
    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
    1. Masthead (page fmi)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320370401

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    17. Brief Clinical Reports
    18. Articles
    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
    1. Incidence of tuberous sclerosis in patients with cardiac rhabdomyoma (pages 443–446)

      Cary O. Harding and Roberta A. Pagon

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370402

  3. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    17. Brief Clinical Reports
    18. Articles
    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
    1. Baller-Gerold syndrome: An 11th case of craniosynostosis and radial aplasia (pages 447–450)

      Jeanne M. Boudreaux, Marc A. Colon, Giovanni D. Lorusso, Elizabeth A. Parro and Mary Z. Pelias

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370403

  4. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    17. Brief Clinical Reports
    18. Articles
    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
    1. “C” trigonocephaly syndrome: Clinical variability and possibility of surgical treatment (pages 451–456)

      F. Lalatta, D. Clerici Bagozzi, M. G. Salmoiraghi, P. Tagliabue, C. Tischer, M. Zollino, C. Di Rocco, G. Neri and J. M. Opitz

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370404

    2. Opitz C syndrome and pseudohypoaldosteronism (pages 457–459)

      Jan De Koster, Eric Legius, Francis De Zegher, Hugo Devlieger, Jean-Pierre Fryns and Ephrem Eggermont

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370405

  5. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    17. Brief Clinical Reports
    18. Articles
    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
    1. C syndrome with apparently normal development (pages 460–462)

      Robert F. Stratton, Norman J. Sykes and Terence W. Hassler

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370406

  6. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    17. Brief Clinical Reports
    18. Articles
    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
    1. “C” trigonocephaly syndrome: Two additional cases (pages 463–464)

      Gianni Camera, Giovanni Serra and Angelo Selicorni

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320370407

  7. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    17. Brief Clinical Reports
    18. Articles
    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
    1. Phenotypic overlap of Ehlers-Danlos syndrome types IV and VIII (pages 465–470)

      Dr. James K. Hartsfield Jr. and Boris G. Kousseff

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370408

  8. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    17. Brief Clinical Reports
    18. Articles
    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
  9. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    17. Brief Clinical Reports
    18. Articles
    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
    1. Terminal deletion 6P23: A case report (pages 475–477)

      M. H. Kormann-Bortolotto, L. M. S. Farah, D. Soares, M. Corbani, R. Müller and A. C. A. Adell

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370410

    2. Aminopterin-like syndrome sine aminopterin associated with translocation involving chromosomes 5 and 10 (pages 478–481)

      Dr. Moy-Fong Chen, Michel Vekemans, K. Meagher-Villemure, Eugene Outerbridge, F. Clarke Fraser and Vazken M. Der Kaloustian

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370411

    3. Dermatoglyphics in the identification of women either with or at risk for breast cancer (pages 482–488)

      Murray H. Seltzer, Chris C. Plato and Kathleen M. Fox

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320370412

  10. Clinico-Pathological Report

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    17. Brief Clinical Reports
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    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
    1. Progressive neurologic deterioration in a nine-year-old white male (pages 489–503)

      Lewis A. Barness, Sunita Chandra, Pamela Kling, Renata Laxova, David B. Allen and Enid Gilbert-Barness

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370413

  11. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    17. Brief Clinical Reports
    18. Articles
    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
    1. Deletion of 16q with prolonged survival and unusual radiographic manifestations (pages 504–509)

      Anthony C. Casamassima, Robert M. Klein, Patrick L. Wilmot, Pauline Brenholz and Lawrence R. Shapiro

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370414

  12. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    17. Brief Clinical Reports
    18. Articles
    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
    1. Follow-up of 16q deletions (page 510)

      Jean-Pierre Fryns

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370415

  13. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    17. Brief Clinical Reports
    18. Articles
    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
    1. Persistent hyperinsulinemic hypoglycemia of infancy (“nesidioblastosis”): Autosomal recessive inheritance in 7 pedigrees (pages 511–515)

      Benjamin Glaser, Moshe Phillip, Rivka Carmi, Ester Lieberman and Heddy Landau

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320370416

  14. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    17. Brief Clinical Reports
    18. Articles
    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
    1. Concurrence of robinow syndrome and Crigler-Najar syndrome in two offspring of first cousins (pages 516–518)

      Hisham Nazer, Thirumazhisai S. Gunasekaran, Nadia A. Sakati and William L. Nyhan

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370417

    2. Congenital heart disease and Robinow syndrome: Coincidence or an additional component of the syndrome? (pages 519–521)

      Steven A. Webber, David S. Wargowski, David Chitayat and George G. S. Sandor

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370418

  15. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    17. Brief Clinical Reports
    18. Articles
    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
    1. Satisfaction with genetic counseling: Dimensions and measurement (pages 522–529)

      Shoshana Shiloh, Orit Avdor and Richard M. Goodman

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320370419

  16. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    17. Brief Clinical Reports
    18. Articles
    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
    1. Tetralogy of Fallot in three sibs (pages 532–533)

      Rainer Pankau, Werner Siekmeyer and Regina Stoffregen

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370421

  17. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
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    17. Brief Clinical Reports
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    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
    1. Application of a flowchart for the detection of lysosomal storage diseases in 105 high-risk Brazilian patients (pages 534–538)

      Maria Luiza Barth, Roberto Giugliani, Sandra L. Goldenfum, Roberta Munarski, Adriana Folberg, Chandra Lekhwani, Christina Slade and Anthony H. Fensom

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370422

    2. New study on the relationship between oral clefts and fetal loss (pages 539–542)

      Beatriz G. Menegotto and Francisco M. Salzano

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370423

  18. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    17. Brief Clinical Reports
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    22. Articles
    23. Letter to the Editors
    1. Monozygotic twins discordant for the Russell-Silver syndrome (pages 543–545)

      Michael Samn, Kathleen Lewis and Bruce Blumberg

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370424

  19. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
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    17. Brief Clinical Reports
    18. Articles
    19. Brief Clinical Reports
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    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
    1. Cohen syndrome and de novo reciprocal translocation t(5;7) (q33.1;p15.1) (pages 546–547)

      Jean-Pierre Fryns, Alice Kleczkowska, Eric Smeets, Paul Thiry, Jaak Geutjens and Herman Van den Berghe

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370425

    2. Euchromatic 16p + heteromorphism: First report in North America (pages 548–550)

      S. M. Jalal, Nancy R. Schneider, Mary K. Kukolich and Golder N. Wilson

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320370426

    3. Sexual discordance in monozygotic twins (pages 551–557)

      Elizabeth J. Perlman, Gail Stetten, Cathy M. Tuck-Müller, Rosann A. Farber, Wilma L. Neuman, Karin J. Blakemore and Grover M. Hutchins

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320370427

    4. Monochorionic diamniotic minimally conjoined twins: A case report (pages 558–561)

      P. J. Weston, E. J. Ives, R. L. H. Honore, G. M. Lees, D. B. Sinclair and D. Schiff

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370428

    5. Roberts syndrome or “X-linked amelia”? (pages 569–572)

      Ruth Gershoni-Baruch, Arie Drugan, Moshe Bronshtein and Etan Z. Zimmer

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370430

  20. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
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    17. Brief Clinical Reports
    18. Articles
    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
  21. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
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    17. Brief Clinical Reports
    18. Articles
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    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors
    1. The syndrome of Möbius sequence, peripheral neuropathy, and hypogonadotropic hypogonadism (pages 578–582)

      Masahiko Kawai, Toru Momoi, Tatsuya Fujii, Shozo Nakano, Yasuko Itagaki and Haruki Mikawa

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320370432

    2. Prenatal diagnosis of Fraser syndrome at 18.5 weeks gestation, with autopsy findings at 19 weeks (pages 583–591)

      G. M. Schauer, L. K. Dunn, L. Godmilow, R. C. Eagle Jr. and A. S. Knisely

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320370433

  22. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Letter to the Editors
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Clinico-Pathological Report
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    17. Brief Clinical Reports
    18. Articles
    19. Brief Clinical Reports
    20. Articles
    21. Brief Clinical Reports
    22. Articles
    23. Letter to the Editors

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