American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

May 1984

Volume 18, Issue 1

Pages fmi–fmi, 1–190

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Letter to the Editor
    6. Errata
    1. Masthead (page fmi)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180101

  2. Genetic Drift

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Letter to the Editor
    6. Errata
    1. You have free access to this content
      I dream of genealogy (pages 1–3)

      Laurence E. Karp

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180102

  3. Articles

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Letter to the Editor
    6. Errata
    1. A Genetic Study of red cell osmotic fragility in Huntington's disease (pages 5–11)

      Dr. Michael K. McCormack, Alice Lazzarini, David Toke and Frederick Lepore

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180103

    2. A second family with autosomal dominant osteosclerosis—type Stanescu (pages 13–18)

      Dr. J. E. Dipierri and J. D. Guzman

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180104

    3. Cat-eye syndrome with unusual marker chromosome probably not chromosome 22 (pages 19–24)

      Dr. Warren Rosenfeld, Ram S. Verma, Ramesh C. Jhaveri and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180105

    4. Prenatal diagnosis of thanatophoric dysplasia at 24 weeks (pages 39–43)

      Dr. Gianni Camera, Danilo Dodero and Sergio De Pascale

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180107

    5. Age at clinical onset and at ultrasonographic detection of adult polycystic kidney disease: Data for genetic counselling (pages 45–53)

      Dr. J. C. Bear, P. McManamon, J. Morgan, R. H. Payne, H. Lewis, M. H. Gault, D. N. Churchill and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180108

    6. Trigonocephaly: A new familial syndrome (pages 55–59)

      Dr. Moshe Frydman, Arieh Kauschansky, Ezra Elian and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180109

    7. Linkage analysis in a large kindred with autosomal dominant transmission of polyglandular autoimmune disease type II (Schmidt syndrome) (pages 61–65)

      Merlin G. Butler, Dr. M. E. Hodes, P. M. Conneally, Angenieta A. Biegel, James C. Wright and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180110

    8. Corneal changes, hyperkeratosis, short stature, brachydactyly, and premature birth: A new autosomal dominant syndrome (pages 67–77)

      Judith K. Stern, Dr. Mark S. Lubinsky, Daniel S. Durrie, John R. Luckasen and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180111

    9. Genetic counseling and reproductive uncertainty (pages 79–88)

      Dr. Dorothy C. Wertz, James R. Sorenson, Timothy C. Heeren and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180112

    10. The dynamics of quantifiable homeostasis. IV: Zero-order homeostasis (pages 99–113)

      Dr. Edmond A. Murphy, William A. Renie and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180114

    11. The natural history of Huntington disease: Possible role of “aging genes” (pages 115–123)

      Lindsay A. Farrer, P. Michael Conneally and Pao-Io Yu

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180115

    12. Duplication of part of chromosome 1q: Clinical report and review of literature (pages 125–134)

      Dr. Virginia V. Michels, Carol Lynn Berseth, John F. O'Brien, Gordon Dewald and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180116

    13. Phenotypic variability in Townes-Brocks syndrome (pages 147–152)

      Dr. João Monteiro de Pina-Neto and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180118

    14. A new lipid storage myopathy observed in individuals with the Ruvalcaba-Myhre-Smith syndrome (pages 163–167)

      Dr. J. H. DiLiberti, A. N. D'Agostino, R. H. A. Ruvalcaba, J. R. Schimschock and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180120

    15. The pathophysiology of neurofibromatosis: IX. Paternal age as a factor in the origin of new mutations (pages 169–176)

      Dr. Vincent M. Riccardi, Christopher E. Dobson II, Ranajit Chakraborty, Catherine Bontke and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180121

  4. Letter to the Editor

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Letter to the Editor
    6. Errata
    1. New hope for the retarded? (pages 183–184)

      Thomas D. Bird and Susan R. Harris

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180123

  5. Errata

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Letter to the Editor
    6. Errata
    1. You have free access to this content
      Erratum (page 185)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180124

    2. You have free access to this content
      Erratum (page 186)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180125

    3. You have free access to this content
      Erratum (page 187)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180126

    4. You have free access to this content
      Erratum (page 188)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180127

    5. You have free access to this content
      Erratum (page 189)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180128

    6. You have free access to this content
      Erratum (page 190)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320180129

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