American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

January 1989

Volume 32, Issue 1

Pages fmi–fmi, 1–147

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

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

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320320101

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. New Syndrome
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Brief Clinical Reports
    14. Articles
    15. Letter to the Editors
    1. Juvenile polyposis: A case with early presentation and death attributable to adenocarcinoma of the pancreas (pages 1–8)

      Dr. Ian R. Walpole, Garry Cullity, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320102

    2. A new Spanish family with Hb Louisville (pages 9–14)

      A. Villegas, J. J. Malcorra, I. Balda, F. Calero, A. Porres, J. L. Alvarez-Sala, D. Espinós, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320103

  3. New Syndrome

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

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. New Syndrome
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Brief Clinical Reports
    14. Articles
    15. Letter to the Editors
    1. Chromosome findings in twins with early-onset autistic disorder (pages 19–21)

      Jan Wahlström, Suzanne Steffenburg, Lars Hellgren, Christopher Gillberg, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320105

    2. New chromosome aberration: Duplication of a large part of chromosome 4q and partial deletion of chromosome 1q (pages 22–26)

      Dr. Paul Merlob, Gertrude Kohn, Aviva Litwin, Ilana Nissenkorn, Mariasa Bath-Miriam Katznelson, Salomon H. Reisner, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320106

    3. Dysmorphogenesis of the mandible, zygoma, and middle ear ossicles in hemifacial microsomia and mandibulofacial dysostosis (pages 27–31)

      Elizabeth D. Kay, C. Neil Kay, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320320107

  5. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. New Syndrome
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Brief Clinical Reports
    14. Articles
    15. Letter to the Editors
    1. Autosomal dominant hypoparathyroidism with intracranial calcification outside the basal ganglia (pages 32–35)

      Dr. D. Ross McLeod, David A. Hanley, Robert G. McArthur, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320108

    2. De novo reciprocal 1p;2q translocation in a child with multiple congenital anomalies/mental retardation syndrome (pages 36–41)

      David Chitayat, Carrie L. Fagerstrom, Dagmar K. Kalousek, Jack Rootman, Glenn P. Taylor, Dr. Judith G. Hall, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320109

  6. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. New Syndrome
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Brief Clinical Reports
    14. Articles
    15. Letter to the Editors
    1. A man with isochromosome Xq Klinefelter syndrome with lack of height increase and normal androgenization (pages 42–44)

      Claude-Lise Richer, Gilles Bleau, Alcide Chapdelaine, Manuela Murer-Orlando, Nicole Lemieux, Marcel Cadotte, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320320110

    2. Common fragile sites in couples with recurrent spontaneous abortions (pages 45–51)

      Dr. Brigitte Schlegelberger, Karen Gripp, Werner Grote, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320111

    3. Clinico-pathological conference: The simultaneous presentation of a Reye-like syndrome in two male sibs (pages 52–59)

      Dr. David B. Allen, S. Anne Hendricks, William H. Perloff, Sunita Chandra, Enid F. Gibert, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320112

  7. New Syndrome

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. New Syndrome
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Brief Clinical Reports
    14. Articles
    15. Letter to the Editors
    1. Two brothers with facial anomalies, microcephaly, hypoplastic genitalia, and a failure of psychomotor development (pages 60–62)

      Dr. K. D. MacDermot, R. M. Winter, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320320113

  8. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. New Syndrome
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Brief Clinical Reports
    14. Articles
    15. Letter to the Editors
    1. Etiologic heterogeneity in dyskeratosis congenita (pages 63–66)

      Dr. G. Shashidhar Pai, Samuel Morgan, Carl Whetsell, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320114

  9. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. New Syndrome
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Brief Clinical Reports
    14. Articles
    15. Letter to the Editors
    1. Macrosomia and mental retardation: Evidence of autosomal dominant inheritance in four generations (pages 67–71)

      L. Mangano, S. Palmeri, M. T. Dotti, F. Moschini, Prof. A. Federico, Giovanni Neri and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320115

    2. On the selection of systems for automated cytogenetic analysis (pages 72–80)

      Dr. Claes Lundsteen, Alice O. Martin and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320320116

  10. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. New Syndrome
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Brief Clinical Reports
    14. Articles
    15. Letter to the Editors
    1. Deletion of terminal portion of 6q: Report of a case with unusual malformations (pages 81–86)

      Dr. Susan Shen-Schwarz, Lydon M. Hill, Urvashi Surti, Sandra Marchese, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320320117

  11. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. New Syndrome
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Brief Clinical Reports
    14. Articles
    15. Letter to the Editors
    1. Ullrich-Turner syndrome and anorexia nervosa (pages 87–89)

      Takehiko Ohzeki, Kazuyo Hayashi, Makoto Higurashi, Keiichi Hanaki, Nobuo Ishitani, Kazuo Shiraki, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320118

  12. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. New Syndrome
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Brief Clinical Reports
    14. Articles
    15. Letter to the Editors
    1. Mild Brachmann–de Lange syndrome: Changes of phenotype with age (pages 90–92)

      Dr. Frank Greenberg, Luther K. Robinson, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320119

  13. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. New Syndrome
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Brief Clinical Reports
    14. Articles
    15. Letter to the Editors
    1. Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome (pages 93–99)

      J. Stephen Bamforth, Claire O. Leonard, Bernard N. Chodirker, David Chitayat, Hilda L. Gritter, Jane A. Evans, Beth Keena, Tapio Pantzar, Jan M. Friedman, Judith G. Hall, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320120

    2. Impaired spermatogenesis is not an obligate expression of receptor-defective androgen resistance (pages 100–104)

      Dr. Leonard Pinsky, Morris Kaufman, Donald W. Killinger, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320121

    3. The genetics of Crohn disease: Complex segregation analysis of a family study with 265 patients with Crohn disease and 5,387 relatives (pages 105–108)

      Wolfgang Küster, Leigh Pascoe, Jochen Purrmann, Sabine Funk, Frank Majewski, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320122

    4. Aplasia of pectoralis major muscle and renal anomalies (pages 109–111)

      Dr. Hardally R. Hegde, Alexander K. C. Leung, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320123

    5. Interstitial deletion of chromosome 22 in a patient with the DiGeorge malformation sequence (pages 112–114)

      J. T. Mascarello, J. F. Bastian, M. C. Jones, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320320124

    6. X-linked cutaneous amyloidosis: Further clinical and pathological observations (pages 115–119)

      M. W. Partington, R. S. A. Prentice, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320125

    7. Autosomal dominant inheritance of small kidneys (pages 120–126)

      Bernard S. Kaplan, Lawrence S. Milner, Sigrid Jequier, Paige Kaplan, Jean-Pierre De Chadarevian, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320126

    8. Renal tubular dysgenesis: Delayed onset of oligohydramnios (pages 127–132)

      Ann E. Swinford, Jay Bernstein, Helga V. Toriello, James V. Higgins, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320127

    9. Tricho-rhino-phalangeal syndrome type I with severe mental retardation due to interstitial deletion of 8q23.3–24.13 (pages 133–135)

      Dr. Yoshifumi Yamamoto, Noriko Oguro, Masutomo Miyao, Masayoshi Yanagisawa, John M. Opitz and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320320128

    10. Neu-Laxova syndrome: Pathological, radiological, and prenatal findings in a stillborn female (pages 136–139)

      Dr. Rosa Russo, Maria D'Armiento, Pasquale Martinelli, Valerio Ventruto, Giovanni Neri and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320129

    11. A girl with the Pitt-Rogers-Danks syndrome (pages 140–141)

      Dr. J. W. E. Oorthuys, E. M. Bleeker-Wagemakers, Giovanni Neri and James F. Reynolds

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320320130

  14. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. New Syndrome
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Brief Clinical Reports
    14. Articles
    15. Letter to the Editors
    1. Rett syndrome: Genetic clues based on mitochondrial changes in muscle (pages 142–144)

      Orvar Eeg-Olofsson, Ali G. H. Al-Zuhair, Dr. Ahmad S. Teebi, Mazen M. N. Al-Essa, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320131

    2. Exclusion of allelism and close linkage between neurofibromatosis and multiple cartilaginous exostoses (page 145)

      G. S. Pai, Steven D. Shapiro, Roderick I. Macpherson, John M. Opitz and James F. Reynolds

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320132

    3. Effectiveness of prevention of cystic fibrosis by artificial insemination by donor can be markedly improved by DNA-analysis of sperm donors (pages 146–147)

      Leo P. ten Kate, Gerard J. te Meerman, Charles H. C. M. Buys, James F. Reynolds and Giovanni Neri

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320320134

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