Search Results - 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 by Ly, Thi Thanh Ha, Ngo, Ngoc Diem, Ngo, Nhung Tuyet, Nguyen, Mai Thi Phuong, Nguyen, Huong Thi Mai, Duong, Truc Ba

    Published 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 by 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

    Published 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 by 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 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 by 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 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 by 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

    Published 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 by 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

    Published 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 by 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 2016
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