Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome
Journal
Taiwanese journal of obstetrics & gynecology
Journal Volume
56
Journal Issue
2
Pages
264
Date Issued
2017-04
Author(s)
Chen, Chih-Ping
Wang, Liang-Kai
Lin, Shuan-Pei
Chern, Schu-Rern
Wu, Peih-Shan
Chen, Yen-Ni
Chen, Shin-Wen
Yang, Chien-Wen
Town, Dai-Dyi
Lee, Meng-Shan
Wang, Wayseen
Subjects
GROWTH-HORMONE THERAPY; TURNER SYNDROME; MULTICENTER TRIAL; HEIGHT GAINS; FINAL HEIGHT; GH TREATMENT; DEFICIENCY; CHILDREN
SDGs
Publisher
ELSEVIER TAIWAN
Type
letter