Endocrine phenotype of 6q16.1–q21 deletion involving SIM1 and Prader–Willi syndrome‐like features
暂无分享,去创建一个
E. Zackai | T. Shaikh | L. Medne | V. Stallings | Ryan Housam | Chirag R. Kapadia | K. Izumi | A. Grimberg | B. Kublaoui
暂无分享,去创建一个
E. Zackai | T. Shaikh | L. Medne | V. Stallings | Ryan Housam | Chirag R. Kapadia | K. Izumi | A. Grimberg | B. Kublaoui