American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

1 April 1993

Volume 46, Issue 1

Pages fmi–fmi, 1–112

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    1. Masthead (page fmi)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320460101

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    1. Cytogenetic and molecular analysis in Angelman syndrome (pages 7–11)

      J. L. Zackowski, R. D. Nicholls, B. A. Gray, A. Bent-Williams, W. Gottlieb, P. J. Harris, M. F. Waters, D. J. Driscoll, R. T. Zori and C. A. Williams

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320460104

    2. Angelman and Prader-Willi syndrome: A magnetic resonance imaging study of differences in cerebral structure (pages 26–33)

      Dr. Christiana M. Leonard, Charles A. Williams, Robert D. Nicholls, O. Frank Agee, Kytja K. S. Voeller, Janice C. Honeyman and Edward V. Staab

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320460107

    3. Communication, cognition, and social interaction in the Angelman syndrome (pages 34–39)

      Kandace A. Penner, Joy Johnston, Barbara H. Faircloth, Patricia Irish and Charles A. Williams

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320460108

    4. Hypopigmentation in Angelman syndrome (pages 40–60)

      Richard A. King, Georgia L. Wiesner, Dewayne Townsend and James G. White

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320460109

    5. Human smooth muscle myosin heavy chain gene mapped to chromosomal region 16q12 (pages 61–67)

      Rumiko Matsuoka, Michihiro C. Yoshida, Yoshiyuki Furutani, Shin-Ichiro Imamura, Naotoshi Kanda, Masashi Yanagisawa, Tomoh Masaki and Atsuyoshi Takao

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320460110

    6. Trisomy 22 and facioauriculovertebral (Goldenhar) sequence (pages 68–71)

      Lisa Kobrynski, David Chitayat, Laila Zahed, David McGregor, Louise Rochon, Seymour Brownstein, Michael Vekemans and Darren L. Albert

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320460111

    7. Characterization of a duplication in the terminal band of 4p by molecular cytogenetics (pages 72–76)

      Dr. Herman E. Wyandt, Jeffrey Milunsky, Terry Lerner, James F. Gusella, Alexander Hou, Marcy MacDonald, Soloman Adekunle and Aubrey Milunsky

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320460112

    8. Identification of a cryptic t(5;7) reciprocal translocation by fluorescent in situ hybridization (pages 77–82)

      Renee Bernstein, Maureen E. Bocian, Mary J. Cain, Ulla Bengtsson and John J. Wasmuth

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320460113

    9. Cytogenetic and molecular identification of a de novo direct duplication of the long arm of chromosome 4(q21.3[RIGHTWARDS ARROW]q31.3) (pages 83–87)

      Anna Jeziorowska, Wlodzimierz Ciesla, George E. Houck Jr., Xiu-Lan Yao, Marsha S. Harris, Barbara Truszczak, Maria Skorski, Lucjusz Jakubowski, Edmund C. Jenkins and Bogdan Kaluzewski

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320460114

    10. Identification, counselling, and outcome of two cases of prenatally diagnosed supernumerary small ring chromosomes (pages 88–94)

      Karen Michalski, Mary Rauer, Nancy Williamson, Anthony Perszyk and Joe J. Hoo

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320460115

  3. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    1. 46, XX, 15p+ documented as dup (17p) by fluorescence in situ hybridization (pages 95–97)

      Nancy B. Spinner, Jaclyn A. Biegel, Lorraine Sovinsky, Donna McDonald-McGinn, Kim Rehberg, Annette H. Parmiter and Elaine H. Zackai

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320460116

  4. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Report
    5. Articles
    1. Method for sequential staining of GTL-banded metaphases with fluorescent-labeled chromosome-specific paint probes (pages 98–103)

      Syed M. Jalal, Mark E. Law, Eric R. Christensen, Jack L. Spurbeck and Gordon W. Dewald

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320460117

    2. Molecular characterization of a complex translocation in a newborn infant (pages 104–108)

      R. S. Verma, R. A. Conte, M. J. Macera, A. S. S. I. Khan, S. Hebi, A. A. Masoud, A. Al Zaman and M. Al Bader

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320460118

    3. Trisomy 22 confirmed by fluorescent in situ hybridization (pages 109–112)

      Dr. Robert F. Stratton, Barbara R. DuPont, Vicki L. Mattern, Robert S. Young, James W. McCourt and Charleen M. Moore

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320460119

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