Douglas R. Stewart, M.D. is an internist who developed an interest in the 9qSTDS during his clinical genetics fellowship at the Children's Hospital of Philadelphia. He is now at the National Institutes of Health in Bethesda, MD, where he has a lab and clinic investigating neurofibromatosis type 1.
Article first published online: 1 OCT 2007
Published 2007 Wiley-Liss, Inc.
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
Special Issue: Subtelomeric Microdeletion Syndromes
Volume 145C, Issue 4, pages 383–392, 15 November 2007
How to Cite
Stewart, D. R. and Kleefstra, T. (2007), The chromosome 9q subtelomere deletion syndrome. Am. J. Med. Genet., 145C: 383–392. doi: 10.1002/ajmg.c.30148
This article is a US Government work and, as such, is in the public domain in the United States of America.
The content of this publication does not necessarily reflect the views or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products or organizations imply endorsement by the U.S. Government.
How to cite this article: Stewart DR, Kleefstra T. 2007. The chromosome 9q subtelomere deletion syndrome. Am J Med Genet Part C Semin Med Genet 145C:383–392.
- Issue published online: 24 OCT 2007
- Article first published online: 1 OCT 2007
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