American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

1 April 1992

Volume 42, Issue 6

Pages fmi–fmi, 761–857

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Editorial
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Letter to the Editors
    1. Masthead (page fmi)

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320420601

  2. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Editorial
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Letter to the Editors
    1. Case of multivertebral anomalies, cloacal dysgenesis, and other anomalies presenting prenatally as cystic kidneys (pages 761–765)

      Michel M. Murr, M.D. Mary H. Waziri, Robert L. Schelper and Monzer Abu-Youself

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320420602

  3. Articles

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Editorial
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Letter to the Editors
    1. Vertebral hypersegmentation in a case of the VATER association (pages 766–770)

      M.D. Eric A. Wulfsberg, Terri L. Phillips-Dawkins and Ronald L. Thomas

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320420603

    2. Cytogenetic and molecular investigation of a balanced Xq13q translocation in a patient with retinoblastoma (pages 771–776)

      Dwight Stambolian, Beatrice Sellinger, Dennis Derrington, Robert Sargent and Dr. Beverly S. Emanuel

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320420604

  4. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Editorial
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Letter to the Editors
    1. The second report of Knobloch syndrome (pages 777–779)

      A. E. Czeizel, P. Göblyös, G. Kustos, E. Mester and E. Paraicz

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320420605

  5. Articles

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Editorial
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Letter to the Editors
    1. Monozygotic twin girls with congenital malformations resembling Fanconi anemia (pages 780–784)

      Steven R. Poole, Ann C. M. Smith, Taru Hays, Loris McGavran and Arleen D. Auerbach

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320420606

    2. Chromosome analysis in spontaneous pregnancy loss: Use of placental villus mesodermal core cell cultures (pages 785–788)

      Giuliana S. Songster, Li Sun, Shih-Chung Chang and Sau W. Cheung

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320420607

    3. Possible new type of oral-facial-digital syndrome with retinal abnormalities: OFDS type (VIII) (pages 789–792)

      F. Gurrieri, V. Sammito, B. Ricci, M. Iossa, A. Bellussi and M.D. G. Neri

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320420608

    4. New familial syndrome of unilateral upper eyelid coloboma, aberrant anterior hairline pattern, and anal anomalies in Manitoba Indians (pages 793–799)

      Sandra L. Marles, Cheryl R. Greenberg, Trivedi V. N. Persaud, E. Paul Shuckett and Dr. Albert E. Chudley

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320420609

  6. Editorial

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Editorial
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Letter to the Editors
    1. Prenatal diagnosis availability (page 800)

      M.D. Mitchell S. Golbus

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320420610

  7. Articles

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Editorial
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Letter to the Editors
    1. Partial gonadal dysgenesis in a patient with a marker Y chromosome (pages 807–812)

      Dr. Patricia Y. Fechner, Kirby D. Smith, Ethylin Wang Jabs, Claude J. Migeon and Gary D. Berkovitz

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320420612

  8. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Editorial
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Letter to the Editors
    1. Autosomal dominant congenital laryngomalacia (pages 813–814)

      M.D. Mordechai Shohat, Yakov Sivan, Ellen Taub and Shmuel Davidson

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320420613

  9. Articles

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Editorial
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Letter to the Editors
    1. Failure of PHA-stimulated i(12p) lymphocytes to divide in Pallister–Killian syndrome (pages 815–819)

      Suzanne L. Thornburg Reeser and Sharon L. Wenger

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320420614

    2. Tissue specificity and stability of mosaicism in Pallister–Killian +i(12p) syndrome: Relevance for prenatal diagnosis (pages 820–824)

      Jean H. Priest, Jean M. Rust and Paul M. Fernhoff

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320420615

    3. Survival of fetuses with 45,X: An instructive case and an hypothesis (pages 825–826)

      Dr. Thaddeus E. Kelly, James E. Ferguson and Wendy Golden

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320420616

    4. High frequency of congenital adrenal hyperplasia (classic 11β-hydroxylase deficiency) among Jews from Morocco (pages 827–834)

      Dr. Ariel Rösler, Esther Leiberman and Tirza Cohen

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320420617

    5. Pentalogy of Cantrell and ectopia cordis, a familial developmental field complex (pages 839–841)

      Rick A. Martin, Christopher Cunniff, Lars Erickson and M.D. Kenneth Lyons Jones

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320420619

  10. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Editorial
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Letter to the Editors
    1. Acrofacial Dysostosis syndromes (page 851)

      José Ignacio Rodríguez, José Palacios and Miguel Urioste

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320420621

    2. Reply to Dr. Rodríguez et al. (page 852)

      M.D. Jean-Pierre Fryns

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320420622

    3. Gastrointestinal and renal malformations associated with prenatal exposure to alcohol and other teratogens (page 853)

      Dr. Jeffrey B. Karasik and Robert W. Marion

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320420623

    4. Reply to Drs. Karasik and Marion (page 854)

      María-Luisa Martínez-Frías and Elvira Rodríguez-Pinilla

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320420624

    5. Genetic analyses on a set of parasitic conjoined twins (page 856)

      M.D. Mark W. Steele, Sharon L. Wenger, Ranjan Deka, John J. Mulvihill and Kanthorn Sukarachana

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320420626

    6. Newly recognized congenital progeroid disorder (page 857)

      M.D. Hans-Rudolf Wiedemann

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320420627

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