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In Memory
Exome sequencing reveals frequent inactivating mutations in ARID1A, ARID1B, ARID2 and ARID4A in microsatellite unstable colorectal cancer
Mar 2, 2025
—
by
coffinsiris-foundation
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Coffin-Siris syndrome: Phenotypic evolution of a novel SMARCA4 mutation
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A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling
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