An extremely rare missense mutation of the androgen receptor gene in a Vietnamese family with complete androgen insensitivity syndrome

por Ha, Thi Minh Thi, Le, Phan Tuong Quynh, Le, Thanh Nha Uyen, Hoang, Thi Thuy Yen
Publicado 2023

An Extremely Rare SRD5A2 Gene c.485A>C Mutation in a Compound Heterozygous Newborn with Disorders of Sex Development First Identified in Vietnam

por Le, Phan Tuong Quynh, Le, Thanh Nha Uyen, Nguyen, Thi Thanh Binh, Nguyen, Minh Thao, Ha, Thi Minh Thi
Publicado 2022

An experience in prenatal diagnosis via QF-PCR of a female child with a 9.9 Mb pure deletion at 18p11.32–11.22

por Le, Thanh Nha Uyen, Nguyen, Viet Nhan, Doan, Thi Duyen Anh, Doan, Huu Nhat Binh, Le, Phan Tuong Quynh, Le, Tuan Linh, Ha, Thi Minh Thi
Publicado 2020