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Identification of de novo mutations for ARID1B haploinsufficiency associated with Coffin-Siris syndrome 1 in three Chinese families via array-CGH and whole exome sequencing https://t.co/CBLZIO7WEX https://t.co/XwoBbVWdWq
Identification of de novo mutations for ARID1B haploinsufficiency associated with Coffin-Siris syndrome 1 in three Chinese families via array-CGH and whole exome sequencing https://t.co/CBLZIO7WEX https://t.co/XwoBbVWdWq