Shashi V et al.De Novo Truncating Variants in ASXL2 are Associated with a Unique and Recognizable Clinical Phenotype. Am J Hum Genet. 2016;99(4):991-999. PMID: 28061364.
ASXL2ASXL2Shashi V et al.De Novo Truncating Variants in ASXL2 are Associated with a Unique and Recognizable Clinical Phenotype. Am J Hum Genet. 2016;99(4):991-999. PMID: 28061364.