American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

May 1986

Volume 24, Issue 1

Pages fmi–fmi, 1–209

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. Letter to the Editors
    1. Masthead (page fmi)

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240101

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Letter to the Editors
    1. Chromosome deletion 1q42-43 (pages 1–6)

      Michael S. Watson, Dr. J. Jay Gargus, Karin J. Blakemore, Sanford N. Katz and Dr. W. Roy Breg

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240102

    2. A comparison of the availability and content of genetic counseling as perceived by hemophilic men and carriers in the U.S.A., Canada, Scotland, and Greece (pages 7–21)

      Prof. Ivana Markova, Charles D. Forbes, Louis M. Aledort, Martin Inwood, Titika Mandalaki, Connie H. Miller, Jane Pittadaki and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240103

    3. Diploid-triploid mosaicism: Report of necropsy findings (pages 23–28)

      Mark J. Pettenati, L. David Mirkin, Dr. David J. Goldstein, John M. Opitz and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240104

    4. Syndrome of short stature, microcephaly, mental retardation, and multiple epiphyseal dysplasia—Lowry-Wood syndrome (pages 33–39)

      Professor Norman C. Nevin, Paul S. Thomas, Jill Hutchinson, John M. Opitz and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240106

    5. The Wiedemann-Beckwith syndrome: Pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivity (pages 41–55)

      Dr. Norio Niikawa, Satoshi Ishikiriyama, Satoshi Takahashi, Akira Inagawa, Hidehumi Tonoki, Yachio Ohta, Naoki Hase, Tsutomu Kamei, Tadashi Kajii, John M. Opitz and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240107

    6. A re-examination of major locus hypotheses for high density lipoprotein cholesterol level using 2,170 persons screened in 55 Utah pedigrees (pages 57–67)

      Sandra J. Hasstedt, K. Owen Ash, Roger R. Williams and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240108

    7. Zellweger syndrome: Diagnostic assays, syndrome delineation, and potential therapy (pages 69–82)

      Golder N. Wilson, Ronald G. Holmes, Joseph Custer, Jeffrey L. Lipkowitz, Joan Stover, Nabanita Datta, Amiya Hajra and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240109

    8. Concurrence of von Willebrand's disease and hemophilia A: Implications for carrier detection and prevalence (pages 83–94)

      Connie H. Miller, Margaret W. Hilgartner, Michael B. Harris, James B. Bussel, Louis M. Aledort and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240110

    9. Persistent hyperplastic primary vitreous and recessive oculo-dento-osseous dysplasia (pages 95–100)

      Elias I. Traboulsi, Bishara M. Faris, Vazken M. Der Kaloustian, John M. Opitz and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240111

    10. The Perlman familial nephroblastomatosis syndrome (pages 101–110)

      Dr. Frank Greenberg, Fernando Stein, Mary V. Gresik, Milton J. Finegold, Robert J. Carpenter, Vincent M. Riccardi, Arthur L. Beaudet, John M. Opitz and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240112

    11. Investigation on genetic heterogeneity in Duchenne muscular dystrophy (pages 111–117)

      Eliete Rabbi-bortolini, Mayana Zatz, John M. Opitz and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240113

    12. A new syndrome of severe upper limb hypoplasia and Müllerian duct anomalies (pages 119–126)

      Fahed Halal, John M. Opitz and Dr. James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240114

    13. Editorial comment on the paper by Crowe and Dickerman: On congenital lymphedema (pages 127–129)

      Dr. John M. Opitz

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240115

  3. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Letter to the Editors
    1. Brief clinical report: A genetic association between microcephaly and lymphedema (pages 131–135)

      Carol A. Crowe, Lois H. Dickerman, John M. Opitz and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240116

  4. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Letter to the Editors
    1. Prenatal diagnosis of the Beckwith-Wiedemann syndrome (pages 137–141)

      Dr. Susan C. Winter, Cynthia J. R. Curry, J. Charles Smith, Stephen Kassel, Linda Miller, Janet Andrea and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240117

    2. Routine amniotic fluid alphafetoprotein assay: Experience with 40,000 pregnancies (pages 143–149)

      Dr. Barbara F. Crandall, Myles Matsumoto, John M. Opitz and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240118

    3. An autosomal recessive mental retardation syndrome with hepatic fibrosis and renal cysts (pages 151–158)

      Dr. Elizabeth Thompson, Michael Baraitser, John M. Opitz and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240119

    4. The genetics of quantifiable homeostasis: I. The general issues (pages 159–169)

      Dr. Edmond A. Murphy, Joseph L. Trojak, John M. Opitz and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240120

    5. Ring chromosome 18 in a mother and son (pages 171–174)

      Dr. Michael A. Donlan, Cynthia R. Dolan, John M. Opitz and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240121

    6. Distal deletion of the long arm of chromosome 6: A specific phenotype ? (pages 175–178)

      Jean-Pierre Fryns, Walter Bettens, Herman Van Den Berghe and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240122

    7. Hexosaminidase A deficiency in adults (pages 179–196)

      Dr. Ruth Navon, Zohar Argov, Amos Frisch, John M. Opitz and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240123

  5. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Letter to the Editors
    1. Letter to the editor: Hemoglobin C disorders in whites (pages 197–198)

      Gino Schilirò, Maria Antonietta Romeo, Giovanna Russo Mancuso, Piera Samperi, Antonio Russo and John M. Opitz

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240124

    2. Letter to the editor: Heterogeneity of β thalassemia (page 199)

      Gino Schilirò, Antonio Russo, John M. Opitz and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240125

    3. Letter to the editor: Ring Y chromosome (pages 201–202)

      Heirie Mendez, John M. Opitz and James F. Reynolds

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240126

    4. Letter to the editor: Are there “innocent” amniotic bands? (pages 207–209)

      Z. Papp, Z. Tóth, K. Csécsei, John M. Opitz, James F. Reynolds and R. H. Lindenbaum

      Article first published online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320240129

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