American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

Supplement: The Developmental Field Concept, Part 2

1986

Volume 25, Issue S2

Pages fmi–fmi, 1–254

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

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

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250601

  2. Editorial Comment

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

    1. Top of page
    2. Masthead
    3. Editorial Comment
    4. Articles
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Letter to the Editors
    10. Articles
    11. Brief Clinical Reports
    1. Current concepts: Vater and other associations: Historical perspectives and modern interpretations (pages 9–16)

      Dr. Mark Lubinsky, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250603

    2. Polycystic kidney and cardiovascular malformation association (pages 17–21)

      Andrew Czeizel, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250604

    3. Caudal deficiency and asplenia anomalies in sibs (pages 23–29)

      Ana Fullana, Dr. Enrique Garcia-Frias, M. Luisa Martinez-Frias, Socorro Razquin, José Quero and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250605

    4. Sibs with the polyasplenia developmental field defect (pages 31–36)

      Dr. Helga V. Toriello, Nicholas Kokx, James V. Higgins, Ronald Hofman, Donald F. Waterman, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250606

    5. An association of caudal malformations arising from a defect in the “axial mesoderm” developmental field (pages 37–44)

      Dr R. J. M. Gardner, M. M. Nelson, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250607

    6. Congenital hypothalamic hamartoma associated with severe midline defect: A developmental field defect. Report of a case (pages 45–52)

      Dr. Raoul C. M. Hennekam, Frits A. Beemer, Franka Van Merrienboer, B. A. Van Ketel, Peter P. G. Kramer, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250608

    7. A cluster of Pallister-Hall syndrome cases, (congenital hypothalamic hamartoblastoma syndrome) (pages 53–63)

      John M. Graham Jr., Richard Saunders, Jonathan Fratkin, Peter Spiegel, Mark Harris, Robert Z. Klein, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250609

    8. Occurrence of holoprosencephaly in chromosome 13 disorders cannot be explained by duplication/deficiency of a single locus (pages 65–72)

      Golder N. Wilson, Majed Dasouki, Mason Barr Jr., John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250610

  4. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Editorial Comment
    4. Articles
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Letter to the Editors
    10. Articles
    11. Brief Clinical Reports
    1. The arhinencephaly field defect (pages 73–76)

      Helga V. Toriello, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250611

  5. Articles

    1. Top of page
    2. Masthead
    3. Editorial Comment
    4. Articles
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Letter to the Editors
    10. Articles
    11. Brief Clinical Reports
    1. Neural tube defects: Heterogeneity and homogeneity (pages 77–87)

      Dr. Mary J. Seller, Dagmar K. Kalousek, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250612

    2. Frontonasal “dysplasia,” cerebral anomalies, and polydactyly: Report of a new syndrome and discussion from a developmental field perspective (pages 89–96)

      Helga V. Toriello, Leonard L. Radecki, Joan Sharda, David Looyenga, Robert Mann, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250613

    3. Fetal alcohol syndrome and DiGeorge anomaly. Critical ethanol exposure periods for craniofacial malformations as illustrated in an animal model (pages 97–112)

      Dr. Kathleen K. Sulik, Malcolm C. Johnston, Paula A. Daft, William E. Russell, Deborah B. Dehart, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250614

    4. The DiGeorge anomaly as a developmental field defect (pages 113–127)

      Edward J. Lammer, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250615

  6. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Editorial Comment
    4. Articles
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Letter to the Editors
    10. Articles
    11. Brief Clinical Reports
    1. Hemifacial microsomia, ipsilateral facial palsy, and malformed auricle in two families: An autosomal dominant malformation (pages 129–133)

      Dr. Meinhard Robinow, James F. Reynolds, Joan Fitzgerald, James A. Bryant and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250616

  7. Articles

    1. Top of page
    2. Masthead
    3. Editorial Comment
    4. Articles
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Letter to the Editors
    10. Articles
    11. Brief Clinical Reports
    1. A patient with median cleft face anomaly and bilateral goldenhar anomaly (pages 135–141)

      Maria A. Musarella, Ian D. Young, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250617

    2. A new autosomal dominant acrofacial dysostosis syndrome (pages 143–150)

      James F. Reynolds, Mary Jane Webb, John M. Opitz and Robert J. Gorlin

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250618

    3. Imperforate anus in 700,000 consecutive liveborn infants (pages 151–161)

      D. Spouge, Dr. P. A. Baird, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250619

    4. Familial diaphragmatic defects. Early prenatal diagnosis and evidence for major gene inheritance (pages 163–176)

      Maureen Bocian, M. Anne Spence, Mary L. Marazita, Ann P. Walker, Daniel L. Weissberg, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250620

    5. Isolated diaphragmatic defect in three sibs (pages 177–181)

      Dr. Helga V. Toriello, Gretchen Landenburger, Saroj J. Kapur, James V. Higgins, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250621

    6. Genetic analysis of cleft lip with or without cleft palate in Chinese kindreds (pages 183–190)

      Michael Melnick, Mary L. Marazita, Dan-Ning Hu, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250622

  8. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Editorial Comment
    4. Articles
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Letter to the Editors
    10. Articles
    11. Brief Clinical Reports
    1. Gollop–Wolfgang complex in a 3-month-old girl (pages 191–194)

      Iosif W. Lurie, Helena G. Ilyina, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250623

  9. Articles

    1. Top of page
    2. Masthead
    3. Editorial Comment
    4. Articles
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Letter to the Editors
    10. Articles
    11. Brief Clinical Reports
    1. Parent to child transmission of the thrombocytopenia absent radius (TAR) syndrome (pages 207–214)

      Richard E. Ward, David Bixler, Arthur J. Provisor, Patricia Bader, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250625

    2. Fibular A/hypoplasia: Review and documentation of the fibular developmental field (pages 215–238)

      Susan O. Lewin, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250626

  10. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Editorial Comment
    4. Articles
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Letter to the Editors
    10. Articles
    11. Brief Clinical Reports
    1. Two sporadic cases of amelia/phocomelia with similar phenotype: Rare and unusually symmetrical form of FFU dysostosis or separate entity? (pages 239–245)

      Nataline B. Kardon, Larry P. Dana, Joan M. Fitzgerald, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250627

    2. FG syndrome in a Brazilian child with additional previously unreported signs (pages 247–254)

      A. Richieri-Costa, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320250628

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