American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

February 1985

Volume 20, Issue 2

Pages fmi–fmi, 209–417, i–i

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    9. Book Review
    10. Articles
    11. Erratum
    1. Masthead (page fmi)

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200201

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    9. Book Review
    10. Articles
    11. Erratum
    1. Paternity testing. 2: Likelihood ratio tests (pages 209–219)

      L. Kaiser and Professor G. A. F. Seber

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200202

    2. Male-to-male transmission of the hypertelorism-hypospadias (BBB) syndrome (pages 221–225)

      Dr. Claude Stoll, André Geraudel, Henri Berland, Marie-Paule Roth, Béatrice Dott, Lewis B. Holmes and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200203

    3. Transmitting balanced translocation carrier information within families: A follow-up study (pages 227–232)

      Lorraine Suslak, David M. Price, Franklin Desposito, John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200204

    4. Syndrome of amelogenesis imperfecta, nephrocalcinosis, impaired renal concentration, and possible abnormality of calcium metabolism (pages 233–243)

      Dr. Mark Lubinsky, Carol Angle, P. Wayne Marsh, C. J. Witkop Jr., John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200205

  3. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    9. Book Review
    10. Articles
    11. Erratum
    1. Interstitial deletion of the long arm of chromosome 10: Del(10)(q11.2q21) (pages 245–248)

      Dr. Jeanette J. A. Holden, E. Athen MacDonald, John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200206

  4. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    9. Book Review
    10. Articles
    11. Erratum
    1. Oto-palato-digital syndrome, type II—an X-linked skeletal dysplasia (pages 249–254)

      Thomas G. Brewster, Ralph S. Lachman, David C. Kushner, Lewis B. Holmes, Robert J. Isler, David L. Rimoin, John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200207

    2. Deletions of proximal 15q and non-classical Prader-Willi syndrome phenotypes (pages 255–263)

      S. Schwartz, S. R. Max, S. R. Panny, Dr. M. M. Cohen, John M. Optiz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200208

    3. Brief cytogenetic report on maternal translocation t(7;9)(p22:p23): Two sibs with duplication 9p and one sib with the balanced translocation (pages 265–269)

      Dra. Anita Wajntal, Claudette H. Gonzalez, Célia P. Koiffmann, Deise H. de Souza, John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200209

  5. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    9. Book Review
    10. Articles
    11. Erratum
    1. Non-mosaic partial tetrasomy and partial trisomy 9 (pages 271–276)

      Dr. Steven D. Shapiro, Kathryn L. Hansen, Christine A. Littlefield, John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200210

  6. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    9. Book Review
    10. Articles
    11. Erratum
    1. The phenotypic and cytogenetic spectrum of partial trisomy 9 (pages 277–282)

      Golder N. Wilson, Anita Raj, Diane Baker, John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200211

    2. Distichiasis, congenital heart defects and mixed peripheral vascular anomalies (pages 283–294)

      Dr. Stanley Goldstein, Qutub H. Qazi, Joseph Fitzgerald, Joseph Goldstein, Anita P. Friedman, Philip Sawyer, John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200212

    3. Segregation and linkage analysis of α-N-acetyl-D-glucosaminidase (NAG) levels in a black family (pages 295–306)

      Dr. M. A. Pericak-Vance, J. M. Vance, R. C. Elston, K. K. Namboodiri, T. A. Fogle, John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200213

    4. X-linked motor-sensory neuropathy type-II with deafness and mental retardation: A new disorder (pages 307–315)

      Dr. F. Susan Cowchock, Serge W. Duckett, Leopold J. Streletz, Leonard J. Graziani, Laird G. Jackson, John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200214

    5. Fetal mortality in sibships with one or more affected members with oral clefts (pages 317–323)

      Dr. Osvaldo Mutchinick, Rubén Lisker, Victoria Babinsky, Miguel Angel Santos, Francisco Mejía, Dolores Saavedra, Cristina Villanueva, John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200215

    6. Familial spinocerebellar degeneration with corneal dystrophy (pages 325–339)

      Vazken M. Der Kaloustian, Nabil I. Jarudi, Muin J. Khoury, Adel K. Afifi, Nadia B. Bahuth, Mary E. Deeb, John Shammas, Muhammad A. Mikati, John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200216

    7. Dup(3)(p2[RIGHTWARDS ARROW]pter) in two families, including one infant with cyclopia (pages 341–348)

      Giorgio Gimelli, Cristina Cuoco, Mario Lituania, Massimo Cordone, Maurizio Aricò, Elena Bianchi, Paola Maraschio, Dr. Orsetta Zuffardi, John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200217

    8. Reproductive counselling for multiple sclerosis patients (pages 349–354)

      Dr. A. D. Sadovnick, P. A. Baird, John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200218

    9. Computerized tomography of the foramen magnum: Achondroplastic values compared to normal standards (pages 355–360)

      Jacqueline T. Hecht, F. William Nelson, Lan J. Butler, William A. Horton, Charles I. Scott Jr, E. Robert Wassman, C. Mark Mehringer, David L. Rimoin, Richard M. Pauli, John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200219

    10. Marker Chromosomes: Cytogenetic characterization and implications for prenatal diagnosis (pages 361–368)

      T. Mohandas, N. Canning, W. Chu, M. B. Passage, C. E. Anderson, M. M. Kaback, John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200220

    11. The centralized prenatal genetics screening program of New York City III: The first 7,000 cases (pages 369–384)

      Peter A. Benn, Lillian Y. F. Hsu, Ann Carlson, Hody L. Tannenbaum, John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200221

    12. Increased adhesiveness of trisomy 21 cells and atrioventricular canal malformations in down syndrome: A stochastic model (pages 385–399)

      Dr. David M. Kurnit, John F. Aldridge, Rumiko Matsuoka, Steven Matthysse, John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200222

  7. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    9. Book Review
    10. Articles
    11. Erratum
    1. Letter to the editor (pages 401–402)

      Indrojit Roy, Moy-Fong Chen, Michel Vekemans, John M. Opitz and James F. Reynolds

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200223

    2. Letter to the editor (pages 403–405)

      Simeon Pollack

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200224

  8. Book Review

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    9. Book Review
    10. Articles
    11. Erratum
  9. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    9. Book Review
    10. Articles
    11. Erratum
    1. In vivo alteration of a mutant human protein using the free thiol cysteamine (pages 409–417)

      William A. Gahl, Richard E. Gregg, Jeffrey M. Hoeg and Edward Fisher

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200226

  10. Erratum

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    9. Book Review
    10. Articles
    11. Erratum
    1. You have free access to this content
      Erratum (page i)

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320200227

SEARCH

SEARCH BY CITATION