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De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype
Shashi, Vandana, Pena, Loren D.M., Kim, Katherine, Burton, Barbara, Hempel, Maja, Schoch, Kelly, Walkiewicz, Magdalena, McLaughlin, Heather M., Cho, Megan, Stong, Nicholas, Hickey, Scott E., Shuss, ChVolume:
100
Langue:
english
Journal:
The American Journal of Human Genetics
DOI:
10.1016/j.ajhg.2016.12.004
Date:
January, 2017
Fichier:
PDF, 53 KB
english, 2017