检索结果 - Ngo, Diem Ngoc

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  1. 1
    AB095. Prenatal diagnosis of Duchenne muscular dystrophy by combining of multiplex Polymerase Chain Reaction and Multiplex Ligation dependent Probe Amplification

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

    出版 2017
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  2. 2
    AB131. Case report: a couple having a child affected with beta thalassemia major and another child with hydrops fetalis

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

    出版 2017
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  3. 3
    AB144. Study on the relationship between MYCN status and other prognostic factors in 41 patients with neuroblastoma

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

    出版 2015
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  4. 4
    AB123. Carrier screening and prenatal diagnosis for α- and β-thalassemia in pregnancies at risk in National Hospital of Pediatrics, Vietnam

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

    出版 2015
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  5. 5
    AB140. Ten years experiences of diagnosis spinal muscular atrophy using molecular techniques

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

    出版 2015
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  6. 6
    Clinical and genetic features of congenital bile acid synthesis defect with a novel mutation in AKR1D1 gene sequencing: Case reports

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

    出版 2022
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  7. 7
    AB080. Genetic findings provide insight of biliary atresia patient complexity

    AB080. Genetic findings provide insight of biliary atresia patient complexity 由 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

    出版 2015
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  8. 8
    Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanism

    Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanism 由 Lam, Wai-Yee, Tang, Clara Sze-Man, So, Man-Ting, Yue, Haibing, Hsu, Jacob Shujui, Chung, Patrick Ho-Yu, Nicholls, John M., Yeung, Fanny, Lee, Chun-Wai Davy, Ngo, Diem Ngoc, Nguyen, Pham Anh Hoa, Mitchison, Hannah M., Jenkins, Dagan, O'Callaghan, Christopher, Garcia-Barceló, Maria-Mercè, Lee, So-Lun, Sham, Pak-Chung, Lui, Vincent Chi-Hang, Tam, Paul Kwong-Hang

    出版 2021
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  9. 9
    RET Mutational Spectrum in Hirschsprung Disease: Evaluation of 601 Chinese Patients

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

    出版 2011
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