American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

September 1985

Volume 22, Issue 1

Pages fmi–fmi, 1–221

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. Editorial Comment
    7. Brief Clinical Report
    8. Articles
    9. Letter to the Editors
    10. Letter to the Editor
    11. Book Review
    1. Masthead (page fmi)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220101

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Editorial Comment
    7. Brief Clinical Report
    8. Articles
    9. Letter to the Editors
    10. Letter to the Editor
    11. Book Review
    1. Clinicopathological conference: An adolescent girl with severe mental impairment and mucopolysacchariduria (pages 1–27)

      Dr. M. Daria Haust, Bruce A. Gordon, Richard Hong, Dr. Joseph H. Choi, L. O. Langer, Jürgen Spranger, John M. Opitz and Enid F. Gilbert

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220102

    2. A de novo translocation, 14q21q, with a microchromosome—14p21p (pages 29–33)

      Dvorah Abeliovich, Miriam Katz, Michael Karplus, Rivka Carmi, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220103

    3. Osteoporosis-pseudoglioma syndrome: Report of three affected sibs and an overview (pages 35–47)

      Dr. Marina Frontali, Chiara Stomeo, Bruno Dallapiccola, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220104

    4. The Greig cephalopolysyndactyly syndrome: Report of a family and review of the literature (pages 59–68)

      Dr. Thomaz Rafael Gollop, Luiz Roberto Fontes, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220106

  3. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Editorial Comment
    7. Brief Clinical Report
    8. Articles
    9. Letter to the Editors
    10. Letter to the Editor
    11. Book Review
    1. Johanson-Blizzard syndrome with normal intelligence (pages 69–73)

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

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220107

  4. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Editorial Comment
    7. Brief Clinical Report
    8. Articles
    9. Letter to the Editors
    10. Letter to the Editor
    11. Book Review
    1. Apical hypertrophic cardiomyopathy in a father and daughter (pages 75–80)

      Dr. Joe Malouf, Habib Ratl, Vazken M. Der Kaloustian, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220108

    2. Serum CK-MB activity in progressive muscular dystrophy: Is it of nosologic value? (pages 81–87)

      Mariz Vainzof, Mayana Zatz, Paulo A. Otto, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220109

  5. Editorial Comment

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Editorial Comment
    7. Brief Clinical Report
    8. Articles
    9. Letter to the Editors
    10. Letter to the Editor
    11. Book Review
    1. The Brachmann-de Lange syndrome (pages 89–102)

      Dr. John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220110

  6. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Editorial Comment
    7. Brief Clinical Report
    8. Articles
    9. Letter to the Editors
    10. Letter to the Editor
    11. Book Review
    1. Pregnancy in a woman with the Brachmann-de Lange syndrome (pages 103–107)

      Gayle A. Mosher, Raymond L. Schulte, Phoebe A. Kaplan, Bruce A. Buehler, Warren G. Sanger, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220111

  7. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Editorial Comment
    7. Brief Clinical Report
    8. Articles
    9. Letter to the Editors
    10. Letter to the Editor
    11. Book Review
    1. Brachmann-de Lange syndrome: Evidence for autosomal dominant inheritance (pages 109–115)

      Luther K. Robinson, Dr. Kenneth Lyons Jones, Eric Wolfsberg, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220112

    2. Further delineation of the dup(3q) syndrome (pages 117–123)

      Dr. 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.1320220113

    3. Deficiency of chromosome 8p21.1[RIGHTWARDS ARROW]8pter: Case report and review of the literature (pages 125–134)

      William B. Dobyns, Gordon W. Dewald, Richard O. Carlson, Douglas D. Mair, Dr. Virginia V. Michels, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220114

    4. An autosomal dominant syndrome of characteristic facial appearance, preauricular pits, fifth finger clinodactyly, and tetralogy of fallot (pages 135–141)

      Dr. Marilyn C. Jones, J. Deane Waldman, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220115

    5. Facioscapulohumeral dystrophy with cochlear hearing loss and tortuosity of retinal vessels (pages 143–147)

      Dr. Maria A. Gieron, Jan K. Korthals, Boris G. Kousseff, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220116

    6. Syndromes with lissencephaly. II: Walker-Warburg and Cerebro-Oculo-Muscular syndromes and a new syndrome with type II lissencephaly (pages 157–195)

      Dr. William B. Dobyns, Joel B. Kirkpatrick, Helen M. Hittner, Frank L. Kretzer, Richard M. Roberts, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220118

  8. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Editorial Comment
    7. Brief Clinical Report
    8. Articles
    9. Letter to the Editors
    10. Letter to the Editor
    11. Book Review
    1. Further comments on the lissencephaly syndromes (pages 197–211)

      Dr. William B. Dobyns, Enid F. Gilbert, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220119

  9. Letter to the Editor

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    6. Editorial Comment
    7. Brief Clinical Report
    8. Articles
    9. Letter to the Editors
    10. Letter to the Editor
    11. Book Review
    1. Risk of down syndrome among relatives of down syndrome individuals (pages 213–214)

      Dr. Ernest B. Hook, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220120

    2. Reply to the letter to the editor by Hook (pages 215–216)

      Janet Tamaren, Dr. Eva Sujansky, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220121

  10. Book Review

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

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