1例新生儿常染色体显性智力障碍21型病例报告
陈兰, 赫纹, 刘玲
Autosomal dominant intellectual disability type 21 in a neonate
CHEN Lan, HE Wen, LIU Ling
中国当代儿科杂志 . 2021, (3): 306 -309 .  DOI: 10.7499/j.issn.1008-8830.2010095