Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2→q11.21)

Chen, Chih-PingChih-PingChenTSANG-MING KOSu, Yi-NingYi-NingSuSu, Jun-WeiJun-WeiSuChen, Yu-TingYu-TingChenLee, Chen-ChiChen-ChiLeeChen, Li-FengLi-FengChenWang, WayseenWayseenWang2023-06-202023-06-202013-031028-4559https://scholars.lib.ntu.edu.tw/handle/123456789/632925enDEPENDENT PROBE AMPLIFICATION; RAPID ANEUPLOIDY DIAGNOSIS; NORMAL DAUGHTER; TRANSLOCATION; CHROMOSOME; REGION; ABNORMALITIES; TRANSMISSION; DELINEATION; PHENOTYPE[SDGs]SDG2Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2→q11.21)journal article10.1016/j.tjog.2012.09.037235482422-s2.0-84878015629WOS:000319025700033https://api.elsevier.com/content/abstract/scopus_id/84878015629