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De novotruncating mutations inASXL3are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome

✍ Scribed by Bainbridge, Matthew N; Hu, Hao; Muzny, Donna M; Musante, Luciana; Lupski, James R; Graham, Brett H; Chen, Wei; Gripp, Karen W; Jenny, Kim; Wienker, Thomas F; Yang, Yaping; Sutton, V REID; Gibbs, Richard A; Ropers, H HILGER

Book ID: 120213400
Publisher: BioMed Central
Year: 2013
Tongue: English
Weight: 956 KB
Volume: 5
Category: Article
ISSN: 1756-994X
DOI: 10.1186/gm415

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