American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

November 1985

Volume 22, Issue 3

Pages fmi–fmi, 449–648

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

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

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220301

  2. Invited Editorial Comment

    1. Top of page
    2. Masthead
    3. Invited Editorial Comment
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Letter to the Editors
    1. Workshop on genetic disorders in the Hutterites—Edmonton, Canada, October 12–13, 1983 (pages 449–451)

      Peter Bowen, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220302

  3. Articles

    1. Top of page
    2. Masthead
    3. Invited Editorial Comment
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Letter to the Editors
    1. History and relevance of the Hutterite population for genetic studies (pages 453–462)

      John A. Hostetler, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220303

    2. Morquio syndrome (MPS IVA) and hypophosphatasia in a Hutterite kindred (pages 463–475)

      Dr. R. B. Lowry, F. F. Snyder, R. L. Wesenberg, G. A. Machin, D. A. Applegarth, K. Morgan, R. J. Carter, J. R. Toone, T. M. Holmes, R. D. Dewar, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220304

    3. Multiplicity of genetic polymorphisms of blood in the Schmiedeleut Hutterites (pages 477–485)

      Prof. Marion Lewis, Hiroko Kaita, Eloise R. Giblett, Jeanne Anderson, Sylvia Philipps, Arthur G. Steinberg, Phyllis J. McAlpine, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220305

    4. Muscular dystrophy in Saskatchewan Hutterites (pages 487–493)

      Dr. M. H. K. Shokeir, B. Rozdilsky, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220306

    5. Juvenile cataract in Hutterites (pages 495–500)

      Dr. M. H. K. Shokeir, R. B. Lowry, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220307

    6. Mandibulofacial dysostosis in hutterite sibs: A possible recessive trait (pages 501–512)

      Dr. R. B. Lowry, K. Morgan, T. M. Holmes, P. J. Metcalf, G. F. Stauffer, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220308

    7. Screening for methylmalonic aciduria in alberta: A voluntary program with particular significance for the Hutterite Brethren (pages 513–519)

      Dr. S. Beatrice Fowlow, Floyd F. Snyder, T. Mary Holmes, Kenneth Morgan, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220309

    8. Hutterite cerebro-osteo-nephrodysplasia: Autosomal recessive trait in a Lehrerleut Hutterite family from Montana (pages 521–529)

      Dr. John M. Opitz, R. Brian Lowry, T. Mary Holmes, Kenneth Morgan and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220310

    9. Congenital contractures, edema, hyperkeratosis, and intrauterine growth retardation: A fatal syndrome in hutterite and mennonite kindreds (pages 531–543)

      Dr. R. B. Lowry, G. A. Machin, K. Morgan, D. Mayock, L. Marx, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220311

    10. Congenital anomalies in the Hutterite population: A preliminary survey and hypothesis (pages 545–552)

      Dr. R. B. Lowry, K. Morgan, T. M. Holmes, S. W. M. Gilroy, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220312

    11. The natural history of familial hypopituitarism (pages 553–566)

      Dr. Robert G. McArthur, John Klassen, Kenneth Morgan, John A. Phillips III, Marvin Bala, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220313

  4. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. Invited Editorial Comment
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Letter to the Editors
    1. Disequilibrium syndrome in montana hutterites (pages 567–569)

      Philip D. Pallister, Dr. John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220314

    2. Neurofibromatosis and fragile-X syndrome in the same patient (pages 571–575)

      Dr. Joyce A. Mitchell, Jane Wray, Karen Michalski, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220315

  5. Articles

    1. Top of page
    2. Masthead
    3. Invited Editorial Comment
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Letter to the Editors
    1. NOR activity and centromere suppression related in a de novo fusion tdic(9;13)(p22;p13) chromosome in a child with del(9p) syndrome (pages 577–584)

      Dr. Art Daniel, Linda Ekblom, Sandra Phillips, Joan M. Fitzgerald, John M. Opitz and Vincent M. Riccardi

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220316

    2. I. Familial hypercholesterolemia with “normal” cholesterol in obligate heterozygotes (pages 585–591)

      Dr. James J. Nora, Randall M. Lortscher, Richard D. Spangler, David W. Bilheimer, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220317

    3. II. Clinical studies in a kindred with a kinetic LDL receptor mutation causing familial hypercholesterolemia (pages 593–598)

      Dr. David W. Bilheimer, Cara East, Scott M. Grundy, James J. Nora, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220318

    4. Microcephaly, hypergonadotropic hypogonadism, short stature, and minor anomalies: A new syndrome (pages 599–608)

      Mohamad A. Mikati, Samir S. Najjar, Itaf F. Sahli, Sylvie Mansour, Dr. Vazken M. Der Kaloustian, Rafik E. Melhem, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220319

  6. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. Invited Editorial Comment
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Letter to the Editors
    1. Familial recurrence of achondroplasia (pages 609–613)

      Dr. J. S. Fitzsimmons, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220320

  7. Articles

    1. Top of page
    2. Masthead
    3. Invited Editorial Comment
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Letter to the Editors
    1. Translocation mosaicism in a woman having multiple miscarriages (pages 615–617)

      Leonard J. Sciorra, Ming-Liang Lee, Gail Cuccurullo, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220321

    2. Primary hypogonadism and partial alopecia in three sibs with Müllerian hypoplasia in the affected females (pages 619–622)

      S. A. Al-Awadi, T. I. Farag, A. S. Teebi, K. Naguib, M. Y. El-Khalifa, Y. Kelani, A. Al-Ansari, Dr. R. N. Schimke, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220322

    3. Gingival fibromatosis with sensorineural hearing loss: An autosomal dominant trait (pages 623–627)

      James K. Hartsfield Jr., Dr. David Bixler, Raymond H. Hazen, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220323

  8. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. Invited Editorial Comment
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Letter to the Editors
    1. Perrault syndrome in sisters (pages 629–631)

      Dennis J. McCarthy, Dr. John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220324

  9. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Invited Editorial Comment
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Letter to the Editors
    1. The cat-eye syndrome (page 633)

      Glenn C. Szalay, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220325

    2. Reply to Dr. Szalay (pages 635–636)

      R. S. Verma, K. A. Babu, W. Rosenfeld, R. C. Jhaveri, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220326

    3. The “Michelin tire baby” syndrome—an autosomal dominant trait (pages 637–638)

      Dr. Norio Niikawa, Satoshi Ishikiriyama, Toshiaki Shikimani, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220327

    4. Familial multiple exostoses—no chromosome 8 deletion observed (pages 639–640)

      Judith G. Hall, R. Douglas Wilson, Dagmar Kalousek and Richard Beauchamp

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220328

    5. Teratogenicity of anticonvulsant drugs (pages 641–643)

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

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220329

    6. Response to lammer and cordero (page 645)

      Thaddeus E. Kelly, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220330

    7. The Marinesco-Sjögren syndrome described a quarter of a century before marinesco (pages 647–648)

      Duane Superneau, Wladimir Wertelecki, Dr. Hans Zellweger, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320220331

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