American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

November 1984

Volume 19, Issue 3

Pages fmi–fmi, 413–622

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Articles
    4. Editorial Comment
    5. Animal Model
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Articles
    11. New Syndrome
    12. Animal Model
    13. Letter to the Editors
    14. Book Reviews
    15. Articles
    1. Masthead (page fmi)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190301

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Editorial Comment
    5. Animal Model
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Articles
    11. New Syndrome
    12. Animal Model
    13. Letter to the Editors
    14. Book Reviews
    15. Articles
    1. Teratogenicity of anticonvulsant drugs. II: A prospective study (pages 435–443)

      Dr. Thaddeus E. Kelly, Pamela Edwards, Marjorie Rein, James Q. Miller and Fritz E. Dreifuss

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190303

    2. Teratogenicity of anticonvulsant drugs. IV: The association of clefting and epilepsy (pages 451–458)

      Dr. Thaddeus E. Kelly, Marjorie Rein and Pamela Edwards

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190305

  3. Editorial Comment

    1. Top of page
    2. Masthead
    3. Articles
    4. Editorial Comment
    5. Animal Model
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Articles
    11. New Syndrome
    12. Animal Model
    13. Letter to the Editors
    14. Book Reviews
    15. Articles
    1. Genetic background: The elusive component in the fetal hydantoin syndrome (pages 459–462)

      Dr. Richard H. Finnell and Gerald F. Chernoff

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190306

  4. Animal Model

    1. Top of page
    2. Masthead
    3. Articles
    4. Editorial Comment
    5. Animal Model
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Articles
    11. New Syndrome
    12. Animal Model
    13. Letter to the Editors
    14. Book Reviews
    15. Articles
    1. Variable patterns of malformation in the mouse fetal hydantoin syndrome (pages 463–471)

      Dr. Richard H. Finnell and Gerald F. Chernoff

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190307

  5. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Editorial Comment
    5. Animal Model
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Articles
    11. New Syndrome
    12. Animal Model
    13. Letter to the Editors
    14. Book Reviews
    15. Articles
    1. The fetal valproate syndrome (pages 473–481)

      Dr. John H. DiLiberti, Peter A. Farndon, Nicholas R. Dennis and Cynthia J. R. Curry

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190308

  6. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. Articles
    4. Editorial Comment
    5. Animal Model
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Articles
    11. New Syndrome
    12. Animal Model
    13. Letter to the Editors
    14. Book Reviews
    15. Articles
    1. Familial recurrence of geleophysic dysplasia (pages 483–486)

      C. P. Koiffmann, A. Wajntal, M. J. M. Ursich and A. A. Pupo

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190309

  7. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Editorial Comment
    5. Animal Model
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Articles
    11. New Syndrome
    12. Animal Model
    13. Letter to the Editors
    14. Book Reviews
    15. Articles
    1. Geleophysic dysplasia (pages 487–499)

      Dr. Jürgen Spranger, Enid F. Gilbert, Sunita Arya, George M. I. Hoganson and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190310

    2. Acrofacial dysplasia resembling geleophysic dysplasia (pages 501–506)

      Dr. J. Spranger, E. F. Gilbert, S. Flatz, M. Burdelski and H. C. Kallfelz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190311

    3. Direct intrachromosomal duplication of 16q and heritable fragile site fra (10) (q25) in the same patient (pages 507–513)

      Dr. Dennis R. Romain, Allan G. Frazer, Letizia M. Columbano-Green, Richard G. Parfitt, Rosalind H. Smythe and Cyril J. Chapman

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190312

    4. Impact of PKU on the reproductive patterns in collaborative study families (pages 515–524)

      MS, MSSW Joan K. Burns, Colleen G. Azen, Bobbye Rouse and Hazel Vespa

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190313

    5. Linkage relationships between a major gene for catechol-o-methyltransferase activity and 25 polymorphic marker systems (pages 525–532)

      A. F. Wilson, R. C. Elston, Dr. R. M. Siervogel, Richard Weinshilboum and L. J. Ward

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190314

    6. Genetic causes of chronic musculoskeletal disease in childhood are common (pages 533–538)

      Diana Gregory, Paige Kaplan and Dr. Charles R. Scriver

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190315

  8. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. Articles
    4. Editorial Comment
    5. Animal Model
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Articles
    11. New Syndrome
    12. Animal Model
    13. Letter to the Editors
    14. Book Reviews
    15. Articles
    1. Gene dosage studies supporting localization of the structural gene for galactose-1-phosphate uridyl transferase (GALT) to band p13 of chromosome 9 (pages 539–543)

      Dr. Ling Yu Shih, Lorraine Suslak, Irit Rosin, Bernard M. Searle and Franklin Desposito

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190316

  9. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Editorial Comment
    5. Animal Model
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Articles
    11. New Syndrome
    12. Animal Model
    13. Letter to the Editors
    14. Book Reviews
    15. Articles
    1. The split-hand and split-foot anomaly in a central African Negro population (pages 545–552)

      D. L. Viljoen and Professor P. Beighton

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190317

    2. Reproduction in XYY males: Two new cases and implications for genetic counseling (pages 553–560)

      F. Grass, J. McCombs, C. I. Scott, R. S. Young and Dr. C. M. Moore

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190318

    3. Clinical and biochemical characteristics of prolidase deficiency in siblings (pages 561–571)

      Dr. Bishara J. Freij, Harvey L. Levy, Gertrud Dudin, Diya' Mutasim, Mary Deeb and Vazken M. Der Kaloustian

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190319

    4. Genetic linkage analysis of epidermolysis bullosa simplex, Köbner type (pages 573–577)

      J. C. Mulley, C. M. Nicholls, D. N. Propert, T. Turner and G. R. Sutherland

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190320

  10. New Syndrome

    1. Top of page
    2. Masthead
    3. Articles
    4. Editorial Comment
    5. Animal Model
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Articles
    11. New Syndrome
    12. Animal Model
    13. Letter to the Editors
    14. Book Reviews
    15. Articles
    1. Apparently new oculo-cerebro-acral syndrome (pages 585–587)

      Dr. Joan F. Atkin and Shivanand Patil

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190322

  11. Animal Model

    1. Top of page
    2. Masthead
    3. Articles
    4. Editorial Comment
    5. Animal Model
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Articles
    11. New Syndrome
    12. Animal Model
    13. Letter to the Editors
    14. Book Reviews
    15. Articles
    1. Biochemical genetics of the Lapland dog model of glycogen storage disease type II (acid α-glucosidase deficiency) (pages 589–598)

      Dr. Hendrik C. Walvoort, Regina G. Slee, Koos J. Sluis, Johan F. Koster and Arnold J. J. Reuser

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190323

  12. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. Editorial Comment
    5. Animal Model
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Articles
    11. New Syndrome
    12. Animal Model
    13. Letter to the Editors
    14. Book Reviews
    15. Articles
    1. Risk of Down's syndrome among second- and third-degree relatives of a proband with trisomy 21 (pages 599–600)

      Leo P. ten Kate, Gerard J. te Meerman and G. J. P. A. Anders

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190324

    2. Response to Dr. ten Kate et al (pages 601–602)

      J. Tamaren, K. Spuhler and E. Sujansky

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190325

    3. Prune belly sequence associated with trisomy 13 (pages 603–604)

      Hertha Beckmann, Helga Rehder and R. Rauskolb

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190326

  13. Book Reviews

    1. Top of page
    2. Masthead
    3. Articles
    4. Editorial Comment
    5. Animal Model
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Articles
    11. New Syndrome
    12. Animal Model
    13. Letter to the Editors
    14. Book Reviews
    15. Articles
  14. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Editorial Comment
    5. Animal Model
    6. Articles
    7. Brief Clinical Report
    8. Articles
    9. Brief Clinical Report
    10. Articles
    11. New Syndrome
    12. Animal Model
    13. Letter to the Editors
    14. Book Reviews
    15. Articles
    1. Ehlers-Danlos syndrome IV due to a novel defect in type III procollagen (pages 607–622)

      Dr. Reed E. Pyeritz, Catherine A. Stolle, Nollaig A. Parfrey and Jeanne C. Myers

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190328

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