Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects

Kuo, Yu-LingYu-LingKuoChen, Chih-PingChih-PingChenWang, Liang-KaiLiang-KaiWangTSANG-MING KOChang, Tung-YaoTung-YaoChangChern, Schu-RernSchu-RernChernWu, Peih-ShanPeih-ShanWuChen, Yu-TingYu-TingChenChang, Shu-YuanShu-YuanChang2023-06-202023-06-202014-061028-4559https://scholars.lib.ntu.edu.tw/handle/123456789/632920To report prenatal diagnosis of 22q11.2 deletion syndrome in a pregnancy with congenital heart defects in the fetus.en22q11.2 deletion syndrome; congenital heart defects; prenatal diagnosis[SDGs]SDG3Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defectsjournal article10.1016/j.tjog.2014.04.021250172792-s2.0-84903995463WOS:000339698400025https://api.elsevier.com/content/abstract/scopus_id/84903995463