American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

February 1989

Volume 32, Issue 2

Pages fmi–fmi, 151–290

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. New Syndrome
    6. Articles
    7. New Syndrome
    8. Brief Clinical Reports
    9. Articles
    10. Conference Report
    11. Abstracts
    12. Letter to the Editors
    13. Rapid Publication Articles
    14. Conference Report
    15. Rapid Publication Articles
    1. You have free access to this content
      Masthead (page fmi)

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320201

  2. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. New Syndrome
    6. Articles
    7. New Syndrome
    8. Brief Clinical Reports
    9. Articles
    10. Conference Report
    11. Abstracts
    12. Letter to the Editors
    13. Rapid Publication Articles
    14. Conference Report
    15. Rapid Publication Articles
    1. Orofaciodigital syndrome type IV: Report of a patient (pages 151–154)

      N. C. Nevin, P. S. Thomas, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320320202

  3. Articles

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. New Syndrome
    6. Articles
    7. New Syndrome
    8. Brief Clinical Reports
    9. Articles
    10. Conference Report
    11. Abstracts
    12. Letter to the Editors
    13. Rapid Publication Articles
    14. Conference Report
    15. Rapid Publication Articles
    1. Mutation rate estimates are not compatible with autosomal dominant inheritance of the dysplastic nevus “syndrome” (pages 155–157)

      Dr. Heiko Traupe, Egon Macher, Henning Hamm, Rudolf Happle, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320203

    2. Inherited diseases in North American Mennonites: Focus on old colony (Chortitza) Mennonites (pages 158–168)

      Dr. M. A. Jaworski, A. Severini, G. Mansour, K. Hennig, J. D. Slater, R. Jeske, J. Schlaut, J. W. Yoon, N. K. Maclaren, G. T. Nepom, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320204

  4. New Syndrome

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. New Syndrome
    6. Articles
    7. New Syndrome
    8. Brief Clinical Reports
    9. Articles
    10. Conference Report
    11. Abstracts
    12. Letter to the Editors
    13. Rapid Publication Articles
    14. Conference Report
    15. Rapid Publication Articles
    1. Growth hormone deficiency, Wormian bones, dextrocardia, brachycamptodactyly, and other midline defects (pages 169–173)

      Robert F. Stratton, Mark W. Parker, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320205

  5. Articles

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. New Syndrome
    6. Articles
    7. New Syndrome
    8. Brief Clinical Reports
    9. Articles
    10. Conference Report
    11. Abstracts
    12. Letter to the Editors
    13. Rapid Publication Articles
    14. Conference Report
    15. Rapid Publication Articles
    1. McKusick-Kaufman syndrome: Report of an instructive family (pages 174–177)

      John D. Vince, Nicole J. Martin, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320206

    2. Holoprosencephaly, ear abnormalities, congenital heart defect, and microphallus in a patient with 11q–mosaicism (pages 178–181)

      Robin A. Helmuth, David D. Weaver, Edward R. Wills, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320320207

    3. Atrial septal defect, ventricular septal defect, and coarctation of the aorta in sibs: An autosomal recessive disorder? (pages 182–183)

      Dale F. Nordenberg, Brian Hanna, Jean-Claude Fouron, Dr. Vazken M. Der Kaloustian, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320208

  6. New Syndrome

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. New Syndrome
    6. Articles
    7. New Syndrome
    8. Brief Clinical Reports
    9. Articles
    10. Conference Report
    11. Abstracts
    12. Letter to the Editors
    13. Rapid Publication Articles
    14. Conference Report
    15. Rapid Publication Articles
    1. A new syndrome with distinct facial and auricular malformations and dominant inheritance (pages 184–186)

      Venancio Simosa, Victor B. Penchaszadeh, Tania Bustos, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320209

  7. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. New Syndrome
    6. Articles
    7. New Syndrome
    8. Brief Clinical Reports
    9. Articles
    10. Conference Report
    11. Abstracts
    12. Letter to the Editors
    13. Rapid Publication Articles
    14. Conference Report
    15. Rapid Publication Articles
    1. Congenital pulmonary atresia with intact ventricular septum, tricuspid insufficiency, and patent ductus arteriosus in two sibs (pages 187–188)

      Nancy L. Eriksen, Louis Buttino Jr., Richard C. Juberg, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320210

  8. Articles

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. New Syndrome
    6. Articles
    7. New Syndrome
    8. Brief Clinical Reports
    9. Articles
    10. Conference Report
    11. Abstracts
    12. Letter to the Editors
    13. Rapid Publication Articles
    14. Conference Report
    15. Rapid Publication Articles
    1. Syndrome of imperforate oropharynx with costovertebral and auricular anomalies (pages 189–191)

      David B. Flannery, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320211

    2. Interstitial long-arm deletion of chromosome 7 and ectrodactyly (pages 192–194)

      Eloiza Helena Tajara, Marileila Varella-Garcia and Antonio Carlos Tonelli Gusson

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320212

    3. Diagnostic criteria for Walker-Warburg syndrome (pages 195–210)

      William B. Dobyns, Roberta A. Pagon, Dawna Armstrong, Cynthia J. R. Curry, Frank Greenberg, Arthur Grix, Lewis B. Holmes, Renata Laxova, Virginia V. Michels, Meinhard Robinow, Roberta L. Zimmerman, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320213

    4. Rhesus sensitization after midtrimester genetic amniocentesis (pages 225–226)

      H. Brandenburg, M. G. J. Jahoda, L. Pijpers, J. W. Wladimiroff, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320320216

  9. Conference Report

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. New Syndrome
    6. Articles
    7. New Syndrome
    8. Brief Clinical Reports
    9. Articles
    10. Conference Report
    11. Abstracts
    12. Letter to the Editors
    13. Rapid Publication Articles
    14. Conference Report
    15. Rapid Publication Articles
  10. Abstracts

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. New Syndrome
    6. Articles
    7. New Syndrome
    8. Brief Clinical Reports
    9. Articles
    10. Conference Report
    11. Abstracts
    12. Letter to the Editors
    13. Rapid Publication Articles
    14. Conference Report
    15. Rapid Publication Articles
  11. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. New Syndrome
    6. Articles
    7. New Syndrome
    8. Brief Clinical Reports
    9. Articles
    10. Conference Report
    11. Abstracts
    12. Letter to the Editors
    13. Rapid Publication Articles
    14. Conference Report
    15. Rapid Publication Articles
    1. 3-M syndrome (page 252)

      David B. Flannery and John M. Opitz

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320220

    2. Comment by Raoul C. M. Hennekam on the letter to the editor by Flannery (page 253)

      Raoul C. M. Hennekam and John M. Opitz

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320221

    3. Reply to Dr. Flannery (page 254)

      J. Spranger and John M. Opitz

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320222

    4. Genital overgrowth in the EMG syndrome (pages 255–256)

      Prof. Dr. Hans-Rudolf Wiedemann, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320320223

    5. Dizygotic twinning in mothers of spina bifida (page 257)

      Dr. H. Journel, Dr. B. Le Marec and John M. Opitz

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320224

    6. Reply to Drs. Journel and LeMarec (pages 258–259)

      Charles E. Boklage and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320320225

    7. No correlation between hyperthermia during pregnancy and Hirschsprung disease in the offspring (pages 260–261)

      Lars T. Larsson, Ludvig Okmian, Ulf Kristoffersson and John M. Opitz

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320226

    8. Antley-Bixler syndrome from a prognostic perspective (pages 262–263)

      C. Dawn DeLozier-Blanchet and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320227

    9. Potential for the prenatal diagnosis of hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome (page 264)

      B. Chadefaux, J. P. Bonnefont, D. Rabier, VE. Shih, J. M. Saudubray, P. Kamoun, Giovanni Neri and James F. Reynold

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320228

    10. Facial anomalies in congenital cutis laxa with retarded growth and skeletal dysplasia (page 265)

      Dr. L. Van Maldergem, G. Ogǔr, M. Yüksel and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320320229

  12. Rapid Publication Articles

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. New Syndrome
    6. Articles
    7. New Syndrome
    8. Brief Clinical Reports
    9. Articles
    10. Conference Report
    11. Abstracts
    12. Letter to the Editors
    13. Rapid Publication Articles
    14. Conference Report
    15. Rapid Publication Articles
    1. Dystrophin immunocytochemistry in muscle culture: Detection of a carrier of Duchenne muscular dystrophy (pages 268–273)

      Af Miranda, U Francke, E Bonilla, G Martucci, B Schmidt, G Salviati and M. Rubin

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320320231

    2. Prenatal exclusion testing for Huntington disease using the polymerase chain reaction (pages 274–276)

      I. McIntosh, Ann Curtis, F. A. Millan, D. J. H. Brock, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320232

  13. Conference Report

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. New Syndrome
    6. Articles
    7. New Syndrome
    8. Brief Clinical Reports
    9. Articles
    10. Conference Report
    11. Abstracts
    12. Letter to the Editors
    13. Rapid Publication Articles
    14. Conference Report
    15. Rapid Publication Articles
  14. Rapid Publication Articles

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. New Syndrome
    6. Articles
    7. New Syndrome
    8. Brief Clinical Reports
    9. Articles
    10. Conference Report
    11. Abstracts
    12. Letter to the Editors
    13. Rapid Publication Articles
    14. Conference Report
    15. Rapid Publication Articles
    1. Human cardiac myosin heavy chain gene mapped within chromosome region 14q11.2[RIGHTWARDS ARROW]q13 (pages 279–284)

      Rumiko Matsuoka, Michihiro C. Yoshida, Naotoshi Kanda, Misa Kimura, Hisashi Ozasa, Atsuyoshi Takao, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320234

    2. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion (pages 285–290)

      J. H. M. Knoll, R. D. Nicholls, R. E. Magenis, J. M. Graham Jr., M. Lalande, S. A. Latt, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320235

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