Clinical and laboratory characteristics of Prader-Willi syndrome

por Thao, Bui Phuong, Dung, Vu Chi, Khanh, Nguyen Ngoc, Ngoc, Can Thi Bich, Ngoc, Ngo Diem, Nhung, Dinh Thi Hong, Lan, An Thuy, Mai, Nguyen Thi, Dat, Nguyen Phu, Hoan, Nguyen Thi
Publicado 2013

Cockayne syndrome without UV-sensitivity in Vietnamese siblings with novel ERCC8 variants

por Duong, Nguyen Thuy, Dinh, Tran Huu, Möhl, Britta S., Hintze, Stefan, Quynh, Do Hai, Ha, Duong Thi Thu, Ngoc, Ngo Diem, Dung, Vu Chi, Miyake, Noriko, Hai, Nong Van, Matsumoto, Naomichi, Meinke, Peter
Publicado 2022

Clinical and genetic features of congenital bile acid synthesis defect with a novel mutation in AKR1D1 gene sequencing: Case reports

por Pham, Anh-Hoa Nguyen, Thi, Kim-Oanh Bui, Thi, Mai-Huong Nguyen, Ngo, Diem-Ngoc, Naritaka, Nakayuki, Nittono, Hiroshi, Hayashi, Hisamitsu, Dao, Trang Thi, Nguyen, Kim-Huong Thi, Nguyen, Hoai-Nghia, Giang, Hoa, Tang, Hung-Sang, Nguyen, Tat-Thanh, Truong, Dinh-Kiet, Tran, Minh-Dien
Publicado 2022