American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

April 1983

Volume 14, Issue 4

Pages fmi–fmi, 603–803

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    9. Book Reviews
    1. You have free access to this content
      Masthead (page fmi)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140401

  2. Genetic Drift

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    9. Book Reviews
  3. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    9. Book Reviews
    1. Autosomal recessive anophthalmia with multiple congenital abnormalities—type Waardenburg (pages 607–615)

      Dr. A. Richieri-Costa, T. R. Gollop, P. G. Otto and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140403

  4. Articles

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    9. Book Reviews
    1. Origin of a paternal (13q; 15q) translocation leading to dup(13q) in two half sibs (pages 617–623)

      Dr. Luis F. De Los Cobos and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140404

    2. The branchio-oto-renal (BOR) syndrome: Report of bilateral renal agenesis in three sibs (pages 625–627)

      Dr. R. Carmi, M. Binshtock, D. Abeliovich, J. Bar-Ziv and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140405

    3. Familial paracentric inversion of 1p (pages 629–634)

      Dennis R. Romain, Letizia M. Columbano-Green, Sally Whyte, Rosalind H. Smythe, Richard G. Parfitt, Owen B. Gebbie, Cyril J. Chapman and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140406

    4. Duplication 8q syndrome due to familial chromosome ins(10;8)(q21;q212q22) (pages 635–646)

      Dr. P. Bowen, P. H. Fitzgerald, R. J. M. Gardner, B. Biederman and A. M. O. Veale

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140407

    5. An X;9 translocation, primary amenorrhea, and hypothalamic dysfunction (pages 647–656)

      H. A. Gardner, J. K. McConnon, M. A. Mackenzie and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140408

    6. Congenital heart anomalies in the trisomy 18 syndrome, with reference to congenital polyvalvular disease (pages 657–668)

      Dr. Rumiko Matsuoka, Kazuaki Misugi, Akiko Goto, Enid F. Gilbert, Masahiko Ando and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140409

    7. Hb F levels, longevity of homozygotes and clinical course of sickle cell anemia in Brazil (pages 669–676)

      Mara H. Hutz, Dr. F. M. Salzano, J. Adams and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140410

    8. Familial agnathia-holoprosencephaly (pages 677–698)

      Dr. Richard M. Pauli, James C. Pettersen, Sunita Arya, Enid F. Gilbert and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140411

    9. Fragile (X) X-linked mental retardation I: Relationship between age and intelligence and the frequency of expression of fragil (X)(q28) (pages 699–712)

      Dr. Albert E. Chudley, Joan Knoll, John W. Gerrard, Lawrence Shepel, Ellen McGahey, Jo Anderson and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140412

    10. The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers (pages 713–724)

      Jane Fishburn, Dr. Gillian Turner, Dr. Art Daniel, Ross Brookwell and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140413

    11. Panostotic fibrous dysplasia: A congenital disorder of bone with unusual facial appearance, bone fragility, hyperphosphatasemia, and hypophosphatemia (pages 725–735)

      David E. C. Cole, F. Clarke Fraser, Francis H. Glorieux, Sigrid Jequier, Pierre J. Marie, Theresa M. Reade, Charles R. Scriver and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140414

    12. Clinical and genetic aspects of antithrombin III deficiency (pages 737–750)

      Dr. Fahed Halal, Guy Quenneville, Suzanne Laurin, Ginette Loulou and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140415

  5. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    9. Book Reviews
    1. Two children with de novo del(9p) (pages 751–757)

      Robert S. Young, Patricia Bader, Catherine G. Palmer, Stephen G. Kaler, Dr. M. E. Hodes and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140416

  6. Articles

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    9. Book Reviews
    1. The dup(3)(p25 [RIGHTWARDS ARROW] pter) syndrome: A case with holoprosencephaly (pages 767–772)

      Dr. Nicole J. Martin, Barry G. Steinberg and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140418

    2. The Kenny-Caffey syndrome: Growth retardation and hypocalcemia in a young boy (pages 773–782)

      W. K. Lee, A. Vargas, J. Barnes and Dr. A. W. Root

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140419

  7. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    9. Book Reviews
    1. Parental coital rates and down syndrome (pages 783–784)

      Dr. William H. James and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140420

    2. Occurrence of down syndrome and human sexual behavior (pages 785–786)

      Iva Milstein-Moscati and Willy Beçak

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140421

    3. Routine amniotic fluid alpha-fetoprotein assays (pages 787–788)

      Dr. Aubrey Milunsky and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140422

    4. Response to Dr. Milunsky (page 789)

      Dr. David A. Luthy and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140423

    5. Reply to Dr. Pinsky (page 793)

      Ira K. Brandt, John C. Knowles and Marilyn J. Bull

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140425

    6. Fragile X Chromosome in normal males (pages 795–796)

      Dr. M. G. Daker

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140426

    7. Rejoinder to Dr. Daker (page 797)

      Frederick Hecht, Peter B. Jacky and Grant R. Sutherland

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320140427

  8. Book Reviews

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    9. Book Reviews

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