Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result

Chen, Chih-PingChih-PingChenTSANG-MING KOWang, Liang-KaiLiang-KaiWangChern, Schu-RernSchu-RernChernWu, Peih-ShanPeih-ShanWuChen, Shin-WenShin-WenChenWu, Fang-TzuFang-TzuWuChen, Li-FengLi-FengChenWang, WayseenWayseenWang2023-06-202023-06-202021-071028-4559https://scholars.lib.ntu.edu.tw/handle/123456789/632898We present partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency (NT) and an abnormal maternal serum screening result.enMaternal serum screening; Nuchal translucency; Partial monosomy 8p; Partial trisomy 15q; aCGHPrenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result10.1016/j.tjog.2021.05.034342478242-s2.0-85107903431WOS:000671884000034https://api.elsevier.com/content/abstract/scopus_id/85107903431