AB095. Prenatal diagnosis of Duchenne muscular dystrophy by combining of multiplex Polymerase Chain Reaction and Multiplex Ligation dependent Probe Amplification

Por Ngo, Manh Tien, Nguyen, Thi Phuong Mai, Ngo, Thi Tuyet Nhung, Nguyen, Thi Mai Huong, An, Thuy Lan, Ngo, Diem Ngoc, Vu, Chi Dung, Bui, Phuong Thao
Publicado no Ann Transl Med (2017)

AB131. Case report: a couple having a child affected with beta thalassemia major and another child with hydrops fetalis

Por Ngo, Thi Tuyet Nhung, Ly, Thi Thanh Ha, Ngo, Diem Ngoc, Nguyen, Thi Phuong Mai, An, Thuy Lan, Nguyen, Thi Mai Huong, Ngo, Manh Tien, Nguyen, Hoang Nam
Publicado no Ann Transl Med (2017)

AB144. Study on the relationship between MYCN status and other prognostic factors in 41 patients with neuroblastoma

Por Vu, Dinh Quang, Van Nguyen, Thi Hong, Phung, Tuyet Lan, Tran, Ngoc Son, Le, Dinh Cong, Hoang, Ngoc Thach, Tran, Tran Thi Chi Mai, Nguyen, Xuan Huy, Ngo, Diem Ngoc
Publicado no Ann Transl Med (2015)

AB123. Carrier screening and prenatal diagnosis for α- and β-thalassemia in pregnancies at risk in National Hospital of Pediatrics, Vietnam

Por Ngo, Diem Ngoc, Ly, Thi Thanh Ha, Ngo, Thi Tuyet Nhung, Nguyen, Thi Phuong Mai, Tran, Thi Hong Ha, Duong, Ba Truc, Tran, Danh Cuong, Le, Thi Thanh Thuy, Lê, Thanh Hai, Tran, Thi Thanh Huong
Publicado no Ann Transl Med (2015)

AB140. Ten years experiences of diagnosis spinal muscular atrophy using molecular techniques

Por Nguyen, Thi Phuong Mai, Nguyen, Thi Mai Huong, Ngo, Manh Tien, Ly, Thi Thanh Ha, Ngo, Thi Tuyet Nhung, An, Thuy Lan, Vu, Dinh Quang, Nguyen, Xuan Huy, Ngo, Diem Ngoc, Bui, Phuong Thao, Nguyen, Ngoc Khanh, Vu, Chi Dung, Tran, Danh Cuong
Publicado no Ann Transl Med (2015)

AB080. Genetic findings provide insight of biliary atresia patient complexity

Por Cheng, Guo, Garcia-Barceló, Maria-Mercè, Chung, Patrick Ho-Yu, Tang, Wai-Kiu, Man Wong, Emily Hoi, Chan, Edwin Kin-Wai, So, Man-Ting, Ngo, Diem Ngoc, Tran, Ngoc Son, Nguyen, Pham Anh Hoa, Sham, Pak-Chung, Cherny, Stacey S., Nicholls, John M., Tam, Paul Kwong-Hang
Publicado no Ann Transl Med (2015)

RET Mutational Spectrum in Hirschsprung Disease: Evaluation of 601 Chinese Patients

Por So, Man-Ting, Leon, Thomas Yuk-Yu, Cheng, Guo, Tang, Clara Sze-Man, Miao, Xiao-Ping, Cornes, Belinda K., Ngo, Diem Ngoc, Cui, Long, Ngan, Elly Sau-Wai, Lui, Vincent Chai-Hang, Wu, Xuan-Zhao, Wang, Bin, Wang, Hualong, Yuan, Zheng-Wei, Huang, Liu-Ming, Li, Long, Xia, Huimin, Zhu, Deli, Liu, Juncheng, Nguyen, Thanh Liem, Chan, Ivy Hau-Yee, Chung, Patrick Ho-Yu, Liu, Xue-Lai, Zhang, Ruizhong, Wong, Kenneth Kak-Yuen, Sham, Pak-Chung, Cherny, Stacey S., Tam, Paul Kwong-Hang, Garcia-Barcelo, Maria-Mercè
Publicado em 2011