近亲家庭双重诊断的罕见病例 : 一例病例报告。
Mesh : Consanguinity Developmental Disabilities / diagnosis Dwarfism / diagnosis genetics Humans Infant Leber Congenital Amaurosis / diagnosis genetics Male Osteochondrodysplasias / diagnosis genetics
来 源: DOI:10.1097/MCD.0000000000000374