American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

September 1984

Volume 19, Issue 1

Pages fmi–fmi, 1–207

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Obituary
    4. Brief Clinical Report
    5. Articles
    6. Invited Editorial Comment
    7. Addendum
    8. Articles
    1. You have free access to this content
      Masthead (page fmi)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190101

  2. Obituary

    1. Top of page
    2. Masthead
    3. Obituary
    4. Brief Clinical Report
    5. Articles
    6. Invited Editorial Comment
    7. Addendum
    8. Articles
    1. In Memoriam: Professor C. O. Carter, MA, DM Oxon, FRCP (pages 1–3)

      Marcus Pembrey

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190102

  3. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. Obituary
    4. Brief Clinical Report
    5. Articles
    6. Invited Editorial Comment
    7. Addendum
    8. Articles
    1. Neural tube defects in dup(11 q) (pages 5–8)

      Dr. P. I. Bader, S. M. Haney, R. A. Munsick, S. R. Schubert and M. E. Hodes

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190103

  4. Articles

    1. Top of page
    2. Masthead
    3. Obituary
    4. Brief Clinical Report
    5. Articles
    6. Invited Editorial Comment
    7. Addendum
    8. Articles
    1. Genetic analysis of cleft lip with or without cleft palate in Danish kindreds (pages 9–18)

      Dr Mary L. Marazita, M. Anne Spence and Michael Melnick

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190104

    2. Pulmonary arteriovenous malformations related to Rendu-Osler-Weber syndrome (pages 19–27)

      Dr. Carolyn M. McCue, Michael Hartenberg and Walter E. Nance

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190105

    3. Tetraploidy: A report of three live-born infants (pages 29–37)

      Dr. Paula R. Scarbrough, Joseph Hersh, Mary K. Kukolich, Andrew J. Carroll, Sara C. Finley, Richard Hochberger, Shirley Wilkerson, F. F. Yen and Becky W. Althaus

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190106

    4. Determination for different severity of anemia in thalassemia: Concordance and discordance among sib pairs (pages 39–44)

      Suthat Fucharoen, Pranee Winichagoon, Pensri Pootrakul and Dr. Prawase Wasi

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190107

    5. Age structure and the distribution of rare genetic diseases (pages 65–79)

      Dr. Shozo Yokoyama and Richard H. Ward

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190109

    6. The tricho-rhino-phalangeal syndrome with exostoses (or Langer-Giedion syndrome): Four additional patients without mental retardation and review of the literature (pages 81–112)

      Dr. Leonard O. Langer Jr., Natalie Krassikoff, Renata Laxova, Mary Scheer-Williams, Lowell D. Lutter, Robert J. Gorlin, Charles G. Jennings and Donald W. Day

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190110

  5. Invited Editorial Comment

    1. Top of page
    2. Masthead
    3. Obituary
    4. Brief Clinical Report
    5. Articles
    6. Invited Editorial Comment
    7. Addendum
    8. Articles
  6. Addendum

    1. Top of page
    2. Masthead
    3. Obituary
    4. Brief Clinical Report
    5. Articles
    6. Invited Editorial Comment
    7. Addendum
    8. Articles
    1. You have free access to this content
      Addendum (page 119)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190112

  7. Articles

    1. Top of page
    2. Masthead
    3. Obituary
    4. Brief Clinical Report
    5. Articles
    6. Invited Editorial Comment
    7. Addendum
    8. Articles
    1. Segregation analysis in reciprocal translocation carriers (pages 137–159)

      Dorene L. Petrosky and D. S. Borgaonkar

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190115

    2. Namaqualand hip dysplasia: An autosomal dominant entity (pages 161–169)

      Prof. Peter Beighton, Gail Christy and I. D. Learmonth

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190116

    3. Opsismodysplasia: A new type of chondrodysplasia with predominant involvement of the bones of the hand and the vertebrae (pages 171–182)

      Dr. Pierre Maroteaux, Victor Stanescu, Ritta Stanescu, Bernard Le Marec, Claude Moraine and Horacio Lejarraga

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190117

    4. Testicular regression in a patient with virilized female phenotype (pages 183–188)

      Carla Rosenberg, Z. Mustacchi, A. Braz, I. J. P. Arnhold, T. H. Chu, J. Carnevale and O. Frota-Pessoa

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190118

    5. Interstitial deletion of chromosome 3p: Report of a patient and delineation of a proximal 3p deletion syndrome (pages 189–193)

      Dr. Giovanni Neri, James F. Reynolds, Joan Westphal, Jeffrey Hinz and Art Daniel

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190119

    6. The Perlman syndrome: Familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies (pages 195–207)

      Giovanni Neri, Maria Enrica Martini-Neri, Ben E. Katz and John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320190120

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