Papers: 10.1186/gm415
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome
Cited by: 128
Author(s): Matthew N. Bainbridge, Hao Hu, Donna M. Muzny, Luciana Musante, James R. Lupski, Brett H. Graham, Wei Chen, Karen W. Gripp, Jenny Kim, Thomas F. Wienker, Yaping Yang, V. Reid Sutton, Richard A. Gibbs, Hans Hilger Ropers
Published: over 13 years ago
Software Mentions 1
Very Likely Science (65)