Rezultati - Ngo, Ngoc Diem

  • Showing 1 - 7 results of 7
Refine Results
  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 od Ly, Thi Thanh Ha, Ngo, Ngoc Diem, Ngo, Nhung Tuyet, Nguyen, Mai Thi Phuong, Nguyen, Huong Thi Mai, Duong, Truc Ba

    Izdano 2015
    Polni tekst Polni tekst
    Text
    Dodaj v priljubljene
    Shranjeno v:
  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 od 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

    Izdano 2015
    Polni tekst Polni tekst
    Text
    Dodaj v priljubljene
    Shranjeno v:
  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 od 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

    Izdano 2017
    Polni tekst Polni tekst
    Text
    Dodaj v priljubljene
    Shranjeno v:
  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 od 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

    Izdano 2017
    Polni tekst Polni tekst
    Text
    Dodaj v priljubljene
    Shranjeno v:
  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 od 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

    Izdano 2020
    Polni tekst Polni tekst Polni tekst
    Text
    Dodaj v priljubljene
    Shranjeno v:
  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 od 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

    Izdano 2018
    Polni tekst Polni tekst Polni tekst
    Text
    Dodaj v priljubljene
    Shranjeno v:
  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 od 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

    Izdano 2016
    Polni tekst Polni tekst Polni tekst
    Text
    Dodaj v priljubljene
    Shranjeno v:

Iskalna orodja: