Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome

Chen, Chih-PingChih-PingChenTSANG-MING KOWang, Liang-KaiLiang-KaiWangLin, Shuan-PeiShuan-PeiLinChern, Schu-RernSchu-RernChernWu, Peih-ShanPeih-ShanWuChen, Yen-NiYen-NiChenChen, Shin-WenShin-WenChenYang, Chien-WenChien-WenYangTown, Dai-DyiDai-DyiTownLee, Meng-ShanMeng-ShanLeeWang, WayseenWayseenWang2023-06-202023-06-202017-041028-4559https://scholars.lib.ntu.edu.tw/handle/123456789/632911enGROWTH-HORMONE THERAPY; TURNER SYNDROME; MULTICENTER TRIAL; HEIGHT GAINS; FINAL HEIGHT; GH TREATMENT; DEFICIENCY; CHILDRENMolecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcomeletter10.1016/j.tjog.2017.01.006284205232-s2.0-85015301955WOS:000418316000030https://api.elsevier.com/content/abstract/scopus_id/85015301955