BLUE SYNDROME ドスベロ Frontiers | Case Report: A Novel Homozygous Mutation in MYF5の詳細情報
Frontiers | Case Report: A Novel Homozygous Mutation in MYF5。HOXA13 and HOXD13 expression during development of the。Novel SETBP1 D874V adjacent to the degron causes canonical。Novel HOXD13 variants in syndactyly type 1b and type 1c, and。ブルーシンドローム 1回読みました即購入⭕️値下げ❌