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Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder

✍ Scribed by Fernandez, B. A.; Roberts, W.; Chung, B.; Weksberg, R.; Meyn, S.; Szatmari, P.; Joseph-George, A. M.; MacKay, S.; Whitten, K.; Noble, B.; Vardy, C.; Crosbie, V.; Luscombe, S.; Tucker, E.; Turner, L.; Marshall, C. R.; Scherer, S. W.


Book ID
121396628
Publisher
BMJ Publishing Group
Year
2009
Tongue
English
Weight
919 KB
Volume
47
Category
Article
ISSN
0022-2593

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