New England Journal of Medicine, volume 362, issue 3, pages 239-252
Williams–Beuren Syndrome
1
Center for Human Genetics, Massachusetts General Hospital, Boston, MA 02114, USA. pober.barbara@mgh.harvard.edu
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Publication type: Journal Article
Publication date: 2010-01-20
Journal:
New England Journal of Medicine
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 158.5
ISSN: 00284793, 15334406
General Medicine
Abstract
Williams–Beuren syndrome, a multisystem disorder caused by the deletion of a chromosome region of 1.5 million to 1.8 million base pairs containing 26 to 28 genes, is a disorder of microdeletion or contiguous gene deletion. This review covers current understanding of the biology of this disorder.
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RIS
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TY - JOUR
DO - 10.1056/NEJMra0903074
UR - https://doi.org/10.1056%2FNEJMra0903074
TI - Williams–Beuren Syndrome
T2 - New England Journal of Medicine
AU - Pober, B.
PY - 2010
DA - 2010/01/20 00:00:00
PB - NEJM Group
SP - 239-252
IS - 3
VL - 362
SN - 0028-4793
SN - 1533-4406
ER -
Cite this
BibTex
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@article{2010_Pober,
author = {B. Pober},
title = {Williams–Beuren Syndrome},
journal = {New England Journal of Medicine},
year = {2010},
volume = {362},
publisher = {NEJM Group},
month = {jan},
url = {https://doi.org/10.1056%2FNEJMra0903074},
number = {3},
pages = {239--252},
doi = {10.1056/NEJMra0903074}
}
Cite this
MLA
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Pober, B.. “Williams–Beuren Syndrome.” New England Journal of Medicine, vol. 362, no. 3, Jan. 2010, pp. 239-252. https://doi.org/10.1056%2FNEJMra0903074.