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Showing results 1 to 3 of 3
Issue Date
Title
Author(s)
2020
Phát hiện đột biến mới trên gen SCN5A gây hội chứng QT kéo dài ở bệnh nhi Việt Nam
Bùi, Chí Bảo
;
Nguyễn, Minh Hiệp
;
Nguyễn, Vương Thảo Vy
;
Ngô, Hà Phương
;
Phạm, Hồ Thuật Khoa
;
Vũ, Bảo Quốc
;
Lê, Thị Thu Thủy
;
Trần, Thị Thanh Nga
;
Nông, Thị Minh Hiền
;
Lương, Thị Thu Nga
;
Bùi, Minh Hoàng
;
Lê, Minh Trọng
;
Nguyễn, Thị Huỳnh Nga
2023
Variants APOA5 p.G185C and p.S19W associated with early-onset severe hypertriglyceridemia-induced pancreatitis and diabetes complications in a Vietnamese girl
Nguyen, Huu Hong Thu
;
Nong, Thuy Linh
;
Ma, Thi Huyen Thuong
;
Nguyen, Thuy Duong
;
Nguyen, Hai Ha
2021
Whole exome sequencing revealed a mutation in COL6A1 associated with ullrich congenital muscular dystrophy
Dinh, Huong Thao
;
Nguyen, Phuong Anh
;
Miyake, Noriko
;
Nong, Van Hai
;
Matsumoto, Naomichi
;
Nguyen, Thuy Duong