expanding the shoc2 mutation associated phenotype of noonan syndrome with loose anagen hair structural brain anomalies and myelofibrosis
本文档由 godzuik6l 分享于2016-12-14 14:40
expanding the shoc2 mutation associated phenotype of noonan syndrome with loose anagen hair structural brain anomalies and myelofibrosis
分享：
君，已阅读到文档的结尾了呢~~