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Browsing by Author Meyn, S
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Showing results 1 to 1 of 1
Title
Author(s)
Issue Date
Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder
Journal:
Journal of Medical Genetics
Fernandez, BA
Roberts, W
Chung, B
Weksberg, R
Meyn, S
Szatmari, P
JosephGeorge, AM
MacKay, S
Whitten, K
Noble, B
Vardy, C
Crosbie, V
Luscombe, S
Tucker, E
Turner, L
Marshall, CR
Scherer, SW
2010