American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

May 1983

Volume 15, Issue 1

Pages fmi–fmi, 1–190

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Letter to the Editors
    8. Book Reviews
    1. Masthead (page fmi)

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320150101

  2. Genetic Drift

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Letter to the Editors
    8. Book Reviews
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      Westering (pages 1–2)

      Laurence E. Karp

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150102

  3. Articles

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Letter to the Editors
    8. Book Reviews
    1. The campomelic syndrome: Review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al in 1971 (pages 3–28)

      Dr. C. Stuart Houston, John M. Opitz, Jürgen W. Spranger, Roderick I. Macpherson, Martin H. Reed, Enid F. Gilbert, Jürgen Herrmann and Albert Schinzel

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320150103

    2. Autosomal dominant partial lipodystrophy associated with Rieger anomaly, short stature, and insulinopenic diabetes (pages 29–38)

      Dr. Dagfinn Aarskog, Leiv Ose, Helene Pande, Nils Eide and John M. Opitz

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150104

    3. Autosomal dominant inheritance of the Aarskog syndrome (pages 39–46)

      Robert E. Grier, Frank H. Farrington, Robert Kendig, Peter Mamunes and John M. Opitz

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150105

    4. Chromosome heteromorphism analysis in cases of disputed paternity (pages 47–55)

      Susan B. Olson, R. Ellen Magenis, Shirley I. Rowe, Everett W. Lovrien and John M. Opitz

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150106

    5. Brachymesomelia-renal syndrome (pages 57–65)

      Dr. Leonard O. Langer Jr., Rikio Nishino, Atsuko Yamaguchi, Yoshimoto Ito, Tsuyoshi Ueke, Hajime Togari, Toshiyuki Kato, John M. Opitz, Enid F. Gilbert, Pierre Maroteaux and Jürgen Spranger

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320150107

    6. Trichoodontoonychial dysplasia—a new meso-ectodermal dysplasia (pages 67–70)

      Dr. Marta Pinheiro, Newton Freire-Maia, Alcyone J. Roth and John M. Opitz

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150108

    7. Previously undescribed syndrome of craniofacial, hand anomalies, and sensorineural deafness (pages 71–77)

      Dr. Annemarie Sommer, Theresa Young-Wee and Thomas Frye

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320150109

    8. Inheritance of Bartter syndrome (pages 79–84)

      Dr. R. Rodrigues Pereira, J. van Wersch and John M. Opitz

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150110

    9. Segregation of HLA in families with oral clefts: Evidence against linkage between isolated cleft palate and HLA (pages 85–88)

      Don C. Van Dyke, Dr. Allen S. Goldman, Richard S. Spielman, Chester M. Zmijewski and John M. Opitz

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150111

    10. Intracranial aneurysms: A report of a large pedigree (pages 89–95)

      Dr. Fahed Halal, Gérard Mohr, Tahmouresse Toussi and S. Napoléon Martinez

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320150112

    11. Discordance for the Kleeblattschädel anomaly in monozygotic twins with thanatophoric dysplasia (pages 97–101)

      Dr. William A. Horton, David J. Harris, Debra L. Collins and John M. Opitz

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150113

    12. Oculogastrointestinal muscular dystrophy (pages 103–112)

      Dr. Victor Ionasescu and John M. Opitz

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150114

    13. Brief report: Linkage between G6PD and fragile-X syndrome (pages 113–119)

      Giorgio Filippi, Antoniettina Rinaldi, Nicoletta Archidiacono, Mariano Rocchi, Ivan Balazs and Dr. Marcello Siniscalco

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320150115

    14. Interstitial deletion 2q31[RIGHTWARDS ARROW]q33 (pages 121–126)

      Dr. Philip D. Buchanan, Robin L. Rhodes, C. Edward Stevenson Jr. and John M. Opitz

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150116

    15. Autosomal dominant recurrent encephalopathy of childhood (pages 127–133)

      Dr. Gerhard Neuhäuser, Jerrold M. Eichner, John M. Opitz, W. DeMyer and M.A. Guggenheim

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320150117

    16. Dominantly inherited syndrome of microcephaly and cleft palate (pages 135–140)

      Dr. Fahed Halal and John M. Opitz

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150118

  4. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Letter to the Editors
    8. Book Reviews
    1. Cebocephaly-holoprosencephaly in a newborn girl with a terminal 7q deletion [46,XX,del(7)(pter[RIGHTWARDS ARROW]q32:)] (pages 141–144)

      Stuart Schwartz, Joann Meekins, Susan R. Panny, Chen-Chih J. Sun, Maimon M. Cohen and John M. Opitz

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150119

  5. Articles

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Letter to the Editors
    8. Book Reviews
    1. Chromosome abnormalities in infants with prune belly anomaly: Association with trisomy 18 (pages 145–148)

      Moshe Frydman, R. Ellen Magenis, T. K. Mohandas, Dr. Michael M. Kaback and John M. Opitz

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150120

  6. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Letter to the Editors
    8. Book Reviews
    1. Serum pyruvate-kinase (PK) activity during pregnancy in potential carriers for duchenne muscular dystrophy (pages 149–151)

      Mayana Zatz, Maria Rita Passos, Eliete Rabbi Bortolini and John M. Opitz

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320150121

    2. Autosomal-recessive aplasia cutis congenita—report of two affected sibs (pages 153–156)

      Helga V. Toriello, James V. Higgins, Donald F. Waterman and John M. Opitz

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320150122

    3. Congenital skin defects and gastrointestinal atresia (page 157)

      Nico J. Leschot

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150123

    4. Monozygotic twins discordant for trisomy 21 or chimeric dizygotic twins? (pages 159–160)

      Simone Gilgenkrantz, Christian Janot, J. G. Rogers, L. Voullaire, H. Gold and John M. Opitz

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320150124

    5. Cerebral gigantism, intestinal polyposis, and pigmentary spotting of the genitalia (page 161)

      Fahed Halal and John M. Opitz

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150125

    6. Nuchal cystic hygroma in a fetus with presumed Roberts syndrome (pages 163–167)

      Dr. John M. Graham Jr., Trent D. Stephens and Thomas H. Shepard

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150126

    7. Chromosome studies in hemifacial microsomia with radial ray defect (pages 169–170)

      Dr. Sterling K. Clarren and Darrel J. Salk

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150127

    8. Maternal age in Duchenne muscular dystrophy (pages 171–173)

      R. M. Winter, M. E. Pembrey and Norikuzu Yasuda

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320150128

    9. Familial extragonadal germ cell tumors (pages 175–176)

      Dr. R. Neil Schimke

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150129

    10. Goldenhar association and cranial defects (pages 177–179)

      Richard M. Pauli, Jack H. Jung and Elspeth W. McPherson

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150130

    11. Lymphocyte capping in limb-girdle muscular dystrophy (pages 181–183)

      Virginia P. Sybert, Patricia I. Bader, Douglas W. Townsend and Patricia S. Conn

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320150131

  7. Book Reviews

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Letter to the Editors
    8. Book Reviews

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