Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities

Chen, Chih-PingChih-PingChenTSANG-MING KOWang, Liang-KaiLiang-KaiWangChern, Schu-RernSchu-RernChernWu, Peih-ShanPeih-ShanWuChen, Shin-WenShin-WenChenLai, Shih-TingShih-TingLaiChuang, Tzu-YunTzu-YunChuangYang, Chien-WenChien-WenYangLee, Chen-ChiChen-ChiLeeWang, WayseenWayseenWang2023-06-202023-06-202018-0210284559https://scholars.lib.ntu.edu.tw/handle/123456789/632896We present prenatal diagnosis and molecular cytogenetic characterization of 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities.en17p13.3 microdeletion; CRK; PAFAH1B1; Prenatal diagnosis; YWHAEPrenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalitiesjournal article10.1016/j.tjog.2017.12.022294588822-s2.0-85040922571https://api.elsevier.com/content/abstract/scopus_id/85040922571