American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

February 1984

Volume 17, Issue 2

Pages fmi–fmi, 395–555

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. Articles
    7. Letter to the Editor
    8. Articles
    9. Letter to the Editor
    10. Book Review
    1. You have free access to this content
      Masthead (page fmi)

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320170201

  2. Genetic Drift

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Letter to the Editor
    6. Articles
    7. Letter to the Editor
    8. Articles
    9. Letter to the Editor
    10. Book Review
    1. The spirit of dysmorphology future (or: Hoyle foiled) (pages 395–398)

      Laurence E. Karp and Maureen Bocian

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320170202

  3. Articles

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Letter to the Editor
    6. Articles
    7. Letter to the Editor
    8. Articles
    9. Letter to the Editor
    10. Book Review
    1. The Tel Hashomer camptodactyly syndrome in a consanguineous Brazilian family (pages 399–406)

      Dr. T. R. Gollop, G. M. D. D. Colletto and John M. Opitz

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320170203

    2. Osteogenesis imperfecta type II delineation of the phenotype with reference to genetic heterogeneity (pages 407–423)

      Dr. D. O. Sillence, K. K. Barlow, A. P. Garber, J. G. Hall and D. L. Rimoin

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320170204

    3. Invited editorial comment: Osteogenesis imperfecta: Update and perspective (pages 429–435)

      Dr. Peter H. Byers, Jeffrey F. Bonadio, Beat Steinmann and John M. Opitz

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320170206

    4. Terminal and interstitial deletions of the long arm of chromosome 7: A review with five new cases (pages 437–450)

      Dr. R. S. Young, D. D. Weaver, M. K. Kukolich, N. A. Heerema, C. G. Palmer, E. L. Kawira, H. A. Bender and John M. Opitz

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320170207

    5. A mild autosomal recessive form of osteopetrosis (pages 451–464)

      Dr. Stephen G. Kahler, Jane A. Burns, Arthur S. Aylsworth and John M. Opitz

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320170208

    6. Ring chromosome 14 and immunoglobulin locus (pages 465–469)

      M. Krawczun, G. Melink, Dr. J. Cervenka and John M. Opitz

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320170209

    7. Familial congenital diaphragmatic defects: Aspects of etiology, prenatal diagnosis, and treatment (pages 471–483)

      Dr. Reijo Norio, Helena Kääriäinen, Juhani Rapola, Ritta Herva and Martti Kekomäki

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320170210

    8. Deletion of chromosome 15 (q11 – 13) in a Prader-Labhart-Willi syndrome clinic population (pages 485–495)

      Dr. Suzanne B. Cassidy, Horace C. Thuline, Vanja A. Holm and John M. Opitz

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320170211

    9. Heterogeneity of prenatal onset hydrocephalus: Management and counseling implications (pages 497–508)

      Dr. Roger A. Williamson, Charles W. Schauberger, Michael W. Varner, Carol A. Aschenbrener and John M. Opitz

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320170212

    10. Recurrence rate for de novo 21q21q translocation Down syndrome: A study of 112 families (pages 523–530)

      Charlotte Steinberg, Dr. Elaine H. Zackai, Deborah L. Eunpu, Michael T. Mennuti, Beverly S. Emanuel and John M. Opitz

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320170214

  4. Letter to the Editor

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Letter to the Editor
    6. Articles
    7. Letter to the Editor
    8. Articles
    9. Letter to the Editor
    10. Book Review
    1. Letter to the editor: Eligibility criteria for amniocentesis (pages 531–533)

      Dr. M. Vekemans and A. Lippman

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320170215

  5. Articles

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Letter to the Editor
    6. Articles
    7. Letter to the Editor
    8. Articles
    9. Letter to the Editor
    10. Book Review
    1. Invited editorial: Genetic triage and genetic counseling (pages 535–538)

      Dr. Ernest B. Hook and John M. Opitz

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320170216

  6. Letter to the Editor

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Letter to the Editor
    6. Articles
    7. Letter to the Editor
    8. Articles
    9. Letter to the Editor
    10. Book Review
    1. Letter to the editor: Response to inivited editorial by Hook (page 539)

      M. Vekemans and A. Lippman

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320170217

    2. Letter to the editor: Familial omphalocele and recurrence risk (pages 541–543)

      Iosif W. Lurie, Helena G. Ilyina and John M. Opitz

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320170218

  7. Articles

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Letter to the Editor
    6. Articles
    7. Letter to the Editor
    8. Articles
    9. Letter to the Editor
    10. Book Review
  8. Letter to the Editor

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Letter to the Editor
    6. Articles
    7. Letter to the Editor
    8. Articles
    9. Letter to the Editor
    10. Book Review
  9. Book Review

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Letter to the Editor
    6. Articles
    7. Letter to the Editor
    8. Articles
    9. Letter to the Editor
    10. Book Review

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