医学
HNF1B型
产前诊断
羊膜穿刺术
胎儿
产科
妊娠期
病理
怀孕
生物
遗传学
基因表达
基因
同源盒
作者
Chih‐Ping Chen,Fang-Tzu Wu,Yen-Ting Pan,Peih-Shan Wu,Wayseen Wang
标识
DOI:10.1016/j.tjog.2023.10.005
摘要
We present prenatal diagnosis and perinatal findings of 17q12 microdeletion encompassing HNF1B in a fetus with bilateral hyperechogenic kidneys on fetal ultrasound and mild renal abnormality after birth, and a review of the literature.
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