檢索結果 - Ngo, Ngoc Diem

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  1. 1
    AB111. HBB: c. -78A>G/nt-28(A>G) associated with Cd 26(A-G) HbE, beta thalassemia variant causes thalassemia intermedia

    AB111. HBB: c. -78A>G/nt-28(A>G) associated with Cd 26(A-G) HbE, beta thalassemia variant causes thalassemia intermedia 由 Ly, Thi Thanh Ha, Ngo, Ngoc Diem, Ngo, Nhung Tuyet, Nguyen, Mai Thi Phuong, Nguyen, Huong Thi Mai, Duong, Truc Ba

    出版 2015
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  2. 2
    AB113. The first genetic study on congenital choledochal dilatation (CCD) implicates extracellular matrix proteins

    AB113. The first genetic study on congenital choledochal dilatation (CCD) implicates extracellular matrix proteins 由 Garcia-Barceló, Maria-Mercè, Wong, John Kwong Leong, Ngo, Ngoc Diem, Tran, Ngoc Son, Nguyen, Thanh Liem, Nguyen, Liem, Sham, Pak, Cherny, Stacey, Tam, Paul

    出版 2015
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  3. 3
    AB072. Double aneuploidy of Down-Turner syndrome and Down-Klinefelter syndrome: case report and review

    AB072. Double aneuploidy of Down-Turner syndrome and Down-Klinefelter syndrome: case report and review 由 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

    出版 2017
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  4. 4
    AB015. Study on pericentric inversion of chromosome 9 and congenital abnormalities in children

    AB015. Study on pericentric inversion of chromosome 9 and congenital abnormalities in children 由 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

    出版 2017
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  5. 5
    A random forest-based framework for genotyping and accuracy assessment of copy number variations

    A random forest-based framework for genotyping and accuracy assessment of copy number variations 由 Zhuang, Xuehan, Ye, Rui, So, Man-Ting, Lam, Wai-Yee, Karim, Anwarul, Yu, Michelle, Ngo, Ngoc Diem, Cherny, Stacey S, Tam, Paul Kwong-Hang, Garcia-Barcelo, Maria-Mercè, Tang, Clara Sze-man, Sham, Pak Chung

    出版 2020
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  6. 6
    Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing

    Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing 由 Tang, Clara SM, Zhuang, Xuehan, Lam, Wai-Yee, Ngan, Elly Sau-Wai, Hsu, Jacob Shujui, Michelle, YU, Man-Ting, SO, Cherny, Stacey S, Ngo, Ngoc Diem, Sham, Pak C, Tam, Paul KH, Garcia-Barcelo, Maria-Mercè

    出版 2018
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  7. 7
    Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes

    Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes 由 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

    出版 2016
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