Prenatal diagnosis of partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31→qter) associated with increased nuchal translucency and abnormal maternal serum biochemistry in the first trimester

Chen, Chih-PingChih-PingChenTSANG-MING KOSu, Yi-NingYi-NingSuHsu, Chin-YuanChin-YuanHsuChen, Yi-YungYi-YungChenSu, Jun-WeiJun-WeiSuChen, Wen-LinWen-LinChenPan, Chen-WenChen-WenPanWang, WayseenWayseenWang2023-06-202023-06-202012-031028-4559https://scholars.lib.ntu.edu.tw/handle/123456789/632928enGENOMIC HYBRIDIZATION CHARACTERIZATION; FETAL ASCITES; DELETION[SDGs]SDG2Prenatal diagnosis of partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31→qter) associated with increased nuchal translucency and abnormal maternal serum biochemistry in the first trimesterletter10.1016/j.tjog.2012.01.029224829872-s2.0-84862801257WOS:000303308600029https://api.elsevier.com/content/abstract/scopus_id/84862801257