Associated Papers
Novel de novo frameshift variant in the ASXL3 gene in a child with microcephaly and global developmental delay.
Wayhelova M et al.
Molecular Medicine Reports, 2019
The Role of Additional Sex Combs-Like Proteins in Cancer.
Micol JB et al.
Cold Spring Harbor Perspectives in Medicine, 2016
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome.
Bainbridge MN et al.
Genome Medicine, 2013
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