report of a patient with a constitutional missense mutation in smarcb1, coffin-siris phenotype, and schwannomatosis
本文档由 ngchi531 分享于2016-12-14 05:33
report of a patient with a constitutional missense mutation in smarcb1, coffin-siris phenotype, and schwannomatosis
君,已阅读到文档的结尾了呢~~