论文信息 - Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion. - 字舞流文

Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion.

E. Zackai | B. Emanuel | D. McDonald-McGinn | D M McDonald-McGinn | B S Emanuel | E H Zackai