Clinical and genetic features of congenital bile acid synthesis defect with a novel mutation in AKR1D1 gene sequencing: Case reports
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Published in Medicine (Baltimore) (24.06.2022)
Published in Medicine (Baltimore) (24.06.2022)
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Published in Annals of human genetics (01.09.2014)
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Screening of the RET gene of Vietnamese Hirschsprung patients identifies 2 novel missense mutations
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Published in Journal of pediatric surgery (01.10.2012)
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Cockayne syndrome without UV-sensitivity in Vietnamese siblings with novel ERCC8 variants
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
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Published in Aging (Albany, NY.) (15.07.2022)
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Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanism
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Published in EBioMedicine (01.09.2021)
Published in EBioMedicine (01.09.2021)
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Published in European journal of human genetics : EJHG (01.06.2018)
Published in European journal of human genetics : EJHG (01.06.2018)
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De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloaca
Hsu, Jacob S J, So, Manting, Tang, Clara S M, Karim, Anwarul, Porsch, Robert M, Wong, Carol, Yu, Michelle, Yeung, Fanny, Xia, Huimin, Zhang, Ruizhong, Cherny, Stacey S, Chung, Patrick H Y, Wong, Kenneth K Y, Sham, Pak C, Ngo, Ngoc Diem, Li, Miaoxin, Tam, Paul K H, Lui, Vincent C H, Garcia-Barcelo, Maria-Mercè
Published in Human molecular genetics (15.01.2018)
Published in Human molecular genetics (15.01.2018)
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Mutation spectrum of ATP7B gene in pediatric patients with Wilson disease in Vietnam
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Distal duplication of chromosome 16q22.1q23.1 in a Vietnamese patient with midface hypoplasia and intellectual disability
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Published in American journal of medical genetics. Part A (01.09.2018)
Published in American journal of medical genetics. Part A (01.09.2018)
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A random forest-based framework for genotyping and accuracy assessment of copy number variations
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Published in NAR genomics and bioinformatics (01.09.2020)
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Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes
Wong, John K L, Campbell, Desmond, Ngo, Ngoc Diem, Yeung, Fanny, Cheng, Guo, Tang, Clara S M, Chung, Patrick H Y, Tran, Ngoc Son, So, Man-Ting, Cherny, Stacey S, Sham, Pak C, Tam, Paul K, Garcia-Barcelo, Maria-Mercè
Published in BMC medical genomics (12.12.2016)
Published in BMC medical genomics (12.12.2016)
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RET mutational spectrum in Hirschsprung disease: evaluation of 601 Chinese patients
So, Man-Ting, Leon, Thomas Yuk-Yu, Cheng, Guo, Tang, Clara Sze-Man, Miao, Xiao-Ping, Cornes, Belinda K, Diem, Ngoc Ngo, 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
Published in PloS one (09.12.2011)
Published in PloS one (09.12.2011)
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Apply MIKE 11 model to study impacts of climate change on water resources and develop adaptation plan in the Mekong Delta, Vietnam: a case of Can Tho city
Ho, Bang Quoc, Nguyen, Khoi Dao, Vu, Khue Hoang Ngoc, Nguyen, Tam Thoai, Nguyen, Hang Thi Thuy, Ngo, Diem Doan Ngoc, Tran, Hien Thi Hong, Le, Phuoc Huu, Nguyen, Quan Hong, Ngo, Quang Xuan, Huynh, Nguyen Thi Thao, Nguyen, Hiep Duc
Published in Environmental monitoring and assessment (01.09.2022)
Published in Environmental monitoring and assessment (01.09.2022)
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Clinical and genetic features of congenital bile acid synthesis defect with a novel mutation in AKR1D1 gene sequencing
Anh-Hoa Nguyen Pham, MD, PhD, Kim-Oanh Bui Thi, MD, Mai-Huong Nguyen Thi, MD, Diem-Ngoc Ngo, MD, Nakayuki Naritaka, MD, Hiroshi Nittono, MD, Hisamitsu Hayashi, MD, Trang Thi Dao, MD, Kim-Huong Thi Nguyen, MD, Hoai-Nghia Nguyen, PhD, Hoa Giang, PhD, Hung-Sang Tang, MD, Tat-Thanh Nguyen, MD, Dinh-Kiet Truong, PhD, Minh-Dien Tran, MD
Published in Medicine (Baltimore) (01.06.2022)
Published in Medicine (Baltimore) (01.06.2022)
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AB131. Case report: a couple having a child affected with beta thalassemia major and another child with hydrops fetalis
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
Published in Annals of translational medicine (01.09.2017)
Published in Annals of translational medicine (01.09.2017)
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AB072. Double aneuploidy of Down-Turner syndrome and Down-Klinefelter syndrome: case report and review
Hoang, Moc Thi Thanh, Dinh, Nhung Thi Hong, Tran, Nga Thi, An, Lan Thuy, Vu, Quang Dinh, Nguyen, Huy Xuan, Ngo, Ngoc Diem, Le, Hai Thanh
Published in Annals of translational medicine (01.09.2017)
Published in Annals of translational medicine (01.09.2017)
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AB015. Study on pericentric inversion of chromosome 9 and congenital abnormalities in children
Le, Lieu Thi, Dinh, Nhung Thi Hong, Hoang, Moc Thi Thanh, Tran, Nga Thi, An, Lan Thuy, Vu, Quang Dinh, Ngo, Ngoc Diem, Le, Hai Thanh
Published in Annals of translational medicine (01.09.2017)
Published in Annals of translational medicine (01.09.2017)
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