American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

1979

Volume 3, Issue 1

Pages fmi–fmi, 1–111

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Editorial Comment
    4. Invited Editorial Comment
    5. Articles
    6. Correspondence
    1. Masthead (page fmi)

      Version of Record online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320030101

  2. Editorial Comment

    1. Top of page
    2. Masthead
    3. Editorial Comment
    4. Invited Editorial Comment
    5. Articles
    6. Correspondence
  3. Invited Editorial Comment

    1. Top of page
    2. Masthead
    3. Editorial Comment
    4. Invited Editorial Comment
    5. Articles
    6. Correspondence
    1. Invited editorial comments (page 6)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320030103

  4. Articles

    1. Top of page
    2. Masthead
    3. Editorial Comment
    4. Invited Editorial Comment
    5. Articles
    6. Correspondence
    1. The training of medical geneticists in Britain (pages 7–9)

      A. W. Johnston and John M. Optiz

      Version of Record online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320030104

    2. Canadian College of Medical Geneticists (pages 11–14)

      James R. Miller and John M. Optiz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320030105

    3. Kaufman oculocerebrofacial syndrome: Case report (pages 15–19)

      Dr. Stanislava B. Jurenka, Jane Evans and John M. Optiz

      Version of Record online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320030106

    4. The summitt syndrome: Observations on a third case (pages 27–33)

      Dr. Clifford J. Sells, James W. Hanson, Judith G. Hall and Robert L. Summitt

      Version of Record online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320030108

    5. Autosomal dominant inheritance of scalp defects with ectrodactyly (pages 35–41)

      R. P. Bonafede and Professor P. Beighton

      Version of Record online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320030109

    6. Inherited interstitial del(Xp) with minimal clinical consequences: With a note on the location of genes controlling phenotypic features (pages 43–58)

      Dr. Riitta Herva, Bogdan Kaluzewski, Albert de la Chapelle and Robert L. Summitt

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320030110

    7. The G syndrome: A case report (pages 59–64)

      Cheryl Rockman Greenberg, Dean Schraufnagel and John M. Optiz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320030111

    8. Mutations affecting pigmentation in man: I. Neuroectodermal melanolysosomal disease (pages 65–80)

      Dr. B. Rafael Elejalde, Jorge Holguin, Aurora Valencia, Enid F. Gilbert, Jaime Molina, Gabriel Marin, Luis A. Arango and Carl J. Witkop

      Version of Record online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320030112

  5. Correspondence

    1. Top of page
    2. Masthead
    3. Editorial Comment
    4. Invited Editorial Comment
    5. Articles
    6. Correspondence
    1. Correspondence (pages 109–111)

      Joan Slack, K. K. Namboodiri and R. C. Elston

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320030115

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