Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia

Chen, Chih-PingChih-PingChenChern, Schu-RernSchu-RernChernWang, Tzu-HaoTzu-HaoWangHsueh, Ding-WeiDing-WeiHsuehLee, Chen-ChiChen-ChiLeeTown, Dai-DyiDai-DyiTownWang, WayseenWayseenWangTSANG-MING KO2023-06-202023-06-202005-060197-3851https://scholars.lib.ntu.edu.tw/handle/123456789/632933To present the prenatal diagnosis and molecular cytogenetic analysis of a fetus with nuchal cystic hygroma and ambiguous genitalia.enAmbiguous genitalia | Chromosome 10q deletion | Chromosome 18q duplication | Cystic hygroma | Prenatal diagnosis[SDGs]SDG14Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitaliajournal article10.1002/pd.1179159660442-s2.0-21844463593https://api.elsevier.com/content/abstract/scopus_id/21844463593