Mutation spectrum of CYP21A2 and correlation between genotype – phenotype in 81 Vietnamese patients with congenital adrenal hyperplasia due to 21-hydroxylase defficiency

por Dung, Vu Chi, Khanh, Tran Van, Fukami, Maki, Phuong, Le Thi, Ha, Nguyen Thi, Liem, Nguyen Thanh, Van, Ta Thanh
Publicado 2013

Three novel mutations in the ATP7B gene of unrelated Vietnamese patients with Wilson disease

por Huong, Nguyen Thi Mai, Lien, Nguyen Thi Kim, Ngoc, Ngo Diem, Mai, Nguyen Thi Phuong, Hoa, Nguyen Pham Anh, Hai, Le Thanh, Van Chi, Phan, Van, Ta Thanh, Van Khanh, Tran, Hoang, Nguyen Huy
Publicado 2018

Case Report: Novel rare mutation c.6353C > G in the ABCA12 gene causing harlequin ichthyosis identified by whole exome sequencing

por Tran, Van Khanh, Diep, Quang Minh, Zilong, Qiu, Phuong, Le Thi, Tran, Hai Anh, Van Tung, Nguyen, Lien, Nguyen Thi Kim, Xuan, Nguyen Thi, Ha, Le Thi, Van Ta, Thanh, Tran, Thinh Huy, Hoang, Nguyen Huy
Publicado 2023

Mutation spectrum of retinoblastoma patients in Vietnam

por Linh, Dao Nguyen Ha, Van Huy, Nguyen, Nguyen, Phuoc‐Dung, Le Thi, Phuong, Tuan, Hoang Anh, Van Nguyen, Trong, Tran, Thu Ha, Tran, Hai Anh, Ta, Thanh Dat, Pham, Tuan L. A., Bui, The‐Hung, Tran, Thinh Huy, Van Ta, Thanh, Tran, Van‐Khanh
Publicado 2023