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Sample Articles
Journal Home Page on Wiley InterScience
EDITOR
John C. Carey- Primary Children's Medical Center, Salt Lake City, Utah, USA
ASSOCIATE EDITORS
- Diana W. Bianchi
- Leslie Biesecker
- M. Michael Cohen, Jr.
- Terry J. Hassold
- Raoul C.M. Hennekam
- Norio Niikawa
- David H. Viskochil
- Rosanna Weksberg
- Leslie Biesecker
NEUROPSYCHIATRIC GENETICS
EDITORS- Ming T. Tsuang
- Stephen V. Faraone
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The American Journal of Medical Genetics covers all biological and medical aspects of genetic disorders. The journal publishes original research on a variety of relevant topics, including clinical genetics, cytogenetics, nosology, prenatal diagnosis of genetic disorders, and molecular, biochemical, and population genetics. In addition, the journal features Part B: Neuropsychiatric Genetics, appearing bimonthly and a thematic guest edited Part C: Seminars in Medical Genetics, appearing quarterly.
READERSHIP
- Medical and human geneticists · pediatricians · genetic counselors · population geneticists · clinical biochemists
INDEXED OR ABSTRACTED IN:
- BIOSIS, Cambridge Scientific Abstracts, Current Clinical Cancer, Current Contents/Life Sciences, Excerpta Medica, Index Medicus, Science Citation Index (ISI) and SCISEARCH Database (ISI)
American Journal of Medical Genetics - Sample Articles
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RAPID PUBLICATIONS
Five additional Costello syndrome patients with rhabdomyosarcoma: Proposal for a tumor screening protocol
Karen W. Gripp, Charles I. Scott Jr., Linda Nicholson, Donna M. McDonald-McGinn, J. Daniel Ozeran, Marilyn C. Jones, Angela E. Lin, Elaine H. Zackai
View Abstract | Full Text PDF (Size: 198K)
Mowat-Wilson syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene
Christiane Zweier, Beate Albrecht, Beate Mitulla, Rolf Behrens, Maike Beese, Gabriele Gillessen-Kaesbach, Hans-Dieter Rott, Anita Rauch
View Abstract | Full Text PDF (Size: 153K)
RESEARCH ARTICLES
Usefulness of high-resolution comparative genomic hybridization (CGH) for detecting and characterizing constitutional chromosome abnormalities
Gro Oddveig Ness, Helle Lybæk, Gunnar Houge
View Abstract | Full Text PDF (Size: 464K)
Amish lethal microcephaly: A new metabolic disorder with severe congenital microcephaly and 2-ketoglutaric aciduria
Richard I. Kelley, Donna Robinson, Erik G. Puffenberger, Kevin A. Strauss, D. Holmes Morton
View Abstract | Full Text PDF (Size: 194K)
Performance of cochlear implant recipients with GJB2-related deafness
Glenn E. Green, Daryl A. Scott, Joshua M. McDonald, Holly F.B. Teagle, Bruce J. Tomblin, Linda J. Spencer, George G. Woodworth, John F. Knutson, Bruce J. Gantz, Val C. Sheffield, Richard J.H. Smith
View Abstract | Full Text PDF (Size: 77K)
CLINICAL REPORT
Sotos syndrome associated with a de novo balanced reciprocal translocation t(5;8)(q35;q24.1)
Kiyoshi Imaizumi, Junko Kimura, Mari Matsuo, Kenji Kurosawa, Mitsuo Masuno, Norio Niikawa, Yoshikazu Kuroki
View Abstract | Full Text PDF (Size: 100K)
Seminars in Medical Genetics
Developmental Genetics of Human Malformations. Edited by John M. Opitz.
For information on submissions to Part B: Neuropsychiatric Genetics, go to Neuropsychiatric Genetics Instructions for Authors
For information on submissions to Part C: Seminars in Medical Genetics, go to Seminars in Medical Genetics Instructions for Authors
American Journal of Medical Genetics - Information for Authors
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For more detail, go to the complete Instructions for Authors