American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

August 1990

Volume 36, Issue 4

Pages fmi–fmi, 381–525

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. Articles
    8. Brief Clinical Reports
    9. Articles
    10. Brief Clinical Reports
    11. Articles
    12. Brief Clinical Reports
    13. Articles
    14. Brief Clinical Reports
    15. Articles
    16. Letter to the Editors
    1. Masthead (page fmi)

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360401

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. Brief Clinical Reports
    11. Articles
    12. Brief Clinical Reports
    13. Articles
    14. Brief Clinical Reports
    15. Articles
    16. Letter to the Editors
    1. Transmission of ring 14 chromosome from mother to two sons (pages 381–385)

      Reuben Matalon, Peggy Supple, Herman Wyandt and Ira M. Rosenthal

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360402

    2. Beukes familial hip dysplasia: An autosomal dominant entity (pages 386–390)

      Prof. H. J. Cilliers and P. Beighton

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320360403

    3. Origin of 46,XY/46,XY,r(19) mosaicism (pages 391–393)

      Jar-Fee Yung, Daniel B. Sobel and Joe J. Hoo

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360404

    4. Interstitial deletion involving most of Yq (pages 394–397)

      James Skare, Helen Drwinga, Herman Wyandt, Johanna VanderSpek, Robert Troxler and Aubrey Milunsky

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360405

  3. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. Brief Clinical Reports
    11. Articles
    12. Brief Clinical Reports
    13. Articles
    14. Brief Clinical Reports
    15. Articles
    16. Letter to the Editors
    1. Two siblings with tel Hashomer camptodactyly and mitral valve prolapse (pages 398–403)

      Dr. Helga V. Toriello, James V. Higgins, Thomas Malvitz and Donald F. Waterman

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360406

    2. Prenatal diagnosis of skeletal dysplasia identified postnatally as hypochondroplasia (pages 404–407)

      Susan M. Jones, Luther K. Robinson and Ralph Sperrazza

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360407

  4. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. Brief Clinical Reports
    11. Articles
    12. Brief Clinical Reports
    13. Articles
    14. Brief Clinical Reports
    15. Articles
    16. Letter to the Editors
    1. Fanconi anemia in black African children (pages 408–413)

      Dr. Lorna G. Macdougall, Michael C. Greeff, Jennifer Rosendorff and Renee Bernstein

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320360408

    2. Parental age in the blepharophimosis, ptosis, epicanthus inversus, telecanthus complex (pages 414–417)

      Dr. Wayne H. Finley, Alston Callahan and Jerry N. Thompson

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360409

    3. Blood serotonin and tryptophan in Tourette syndrome (pages 418–430)

      David E. Comings

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320360410

  5. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. Brief Clinical Reports
    11. Articles
    12. Brief Clinical Reports
    13. Articles
    14. Brief Clinical Reports
    15. Articles
    16. Letter to the Editors
    1. Hutchinson-Gilford progeria: Familial occurrence (pages 431–433)

      Dr. H. Parkash, S. S. Sidhu, R. Raghavan and R. N. Deshmukh

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360411

  6. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. Brief Clinical Reports
    11. Articles
    12. Brief Clinical Reports
    13. Articles
    14. Brief Clinical Reports
    15. Articles
    16. Letter to the Editors
    1. Apparent postnatal onset of some manifestations of the Wiedemann-Beckwith syndrome (pages 434–439)

      David Chitayat, Avi Rothchild, Emily Ling, J. M. Friedman, Robert M. Couch, Siu-Li Yong, Virginia J. Baldwin and Judith G. Hall

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360412

    2. Boomerang dysplasia (pages 440–443)

      Dr. I. Winship, B. Cremin and P. Beighton

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360413

    3. Enamel defects: A developmental marker for hemifacial microsomia (pages 444–448)

      David C. Johnsen, Barbara M. Weissman, Gail S. Murray and Dr. Arthur B. Zinn

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360414

    4. Transabdominal chorionic villus sampling in a multiple pregnancy at risk of argininosuccinic aciduria: A case report (pages 449–450)

      Dr. Leen Pijpers, Wim J. Kleijer, Annette Reuss, Milena G. J. Jahoda, Frans J. Los, Eva S. Sachs and Juriy W. Wladimiroff

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320360415

  7. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. Brief Clinical Reports
    11. Articles
    12. Brief Clinical Reports
    13. Articles
    14. Brief Clinical Reports
    15. Articles
    16. Letter to the Editors
    1. Multiple gastrointestinal atresias with imperforate anus: Pathology and pathogenesis (pages 451–455)

      Dr. Susan Shen-Schwarz and Rosanne Fitko

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360416

  8. Articles

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

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
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    10. Brief Clinical Reports
    11. Articles
    12. Brief Clinical Reports
    13. Articles
    14. Brief Clinical Reports
    15. Articles
    16. Letter to the Editors
    1. Rapp-Hodgkin syndrome: Report of a Brazilian family (pages 463–466)

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

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360418

  10. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. Brief Clinical Reports
    11. Articles
    12. Brief Clinical Reports
    13. Articles
    14. Brief Clinical Reports
    15. Articles
    16. Letter to the Editors
    1. Mutation analysis of an Ashkenazi Jewish family with gaucher disease in three successive generations (pages 467–472)

      Edwin H. Kolodny, Nurit Firon, Nurit Eyal and Mia Horowitz

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360419

  11. Brief Clinical Reports

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

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. Brief Clinical Reports
    11. Articles
    12. Brief Clinical Reports
    13. Articles
    14. Brief Clinical Reports
    15. Articles
    16. Letter to the Editors
    1. Fraser syndrome with renal agenesis in two consanguineous Turkish families (pages 477–479)

      C. Francannet, P. Lefrançois, P. Dechelotte, E. Robert, G. Malpuech and J. M. Robert

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360421

    2. Abnormal maternal serum levels of human chorionic gonadotropin free subunits in trisomy 18 (pages 480–483)

      Mehmet Ozturk, Aubrey Milunsky, Bruno Brambati, E. S. Sachs, Susan L. Miller and Jack R. Wands

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360422

    3. Cephalometric analysis of the Prader-Willi syndrome (pages 484–487)

      Robert Schaedel, Andrew E. Poole and Suzanne B. Cassidy

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360423

    4. Bone dysplasias: The prenatal diagnostic challenge (pages 488–494)

      Luis F. Escobar, David Bixler, David D. Weaver, Lillie-Mae Padilla and Alan Golichowski

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320360424

    5. Expanded spectrum of findings in Marden-Walker syndrome (pages 495–499)

      George P. Giacoia and Ramon Pineda

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360425

    6. Partial trisomy 18 with minimal anomalies: Lack of correspondence between phenotypic manifestations and triplicated loci along chromosome 18 (pages 506–510)

      Golder N. Wilson, Karen B. Heller, Roy D. Elterman and Nancy R. Schneider

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320360427

  13. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. Brief Clinical Reports
    11. Articles
    12. Brief Clinical Reports
    13. Articles
    14. Brief Clinical Reports
    15. Articles
    16. Letter to the Editors
    1. Ambiguous genitalia in the Proteus syndrome (pages 511–512)

      Dr. Moshe Frydman, Arieh Kauschansky and Itzhak Varsano

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320360428

  14. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. Brief Clinical Reports
    11. Articles
    12. Brief Clinical Reports
    13. Articles
    14. Brief Clinical Reports
    15. Articles
    16. Letter to the Editors
    1. Trisomy 13 syndrome and neural tube defects (pages 513–516)

      Dr. José Ignacio Rodríguez, Marcial García, Carmen Morales, Ana Morillo and Alicia Delicado

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360429

  15. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. Brief Clinical Reports
    11. Articles
    12. Brief Clinical Reports
    13. Articles
    14. Brief Clinical Reports
    15. Articles
    16. Letter to the Editors
    1. Characteristics relating to Weyers syndrome (page 517)

      Maria Mercedes de Elejalde and B. Rafael Elejalde

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320360430

    2. Reply to de Elejalde and Elejalde (page 518)

      Dr. Nakamichi Saito

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360431

    3. Femoral duplication and the developmental field (pages 521–522)

      Dr. R. A. Pfeiffer, J. Suess and K. M. Schrott

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360433

    4. Chromosome 5 variation (page 523)

      Margaret Fitchett

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320360434

    5. Birth prevalence of Poland sequence and proportion of its familial cases (page 524)

      Andrew Czeizel, Márta Vitéz and Widukind Lenz

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360435

    6. Agnathia-Holoprosencephaly: A midline malformation association (page 525)

      Raoul C. M. Hennekam

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320360436

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