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  • DARUI SERVICE
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    Scientific research and service
    Scientific research and service
    8th
    王元麗,唐明珠,楊學(xué)習. 11339例孕婦無(wú)創(chuàng )產(chǎn)前檢測結果對比分析. 分子診斷與治療雜志[J],2016,8(6),363-366.
    Link
    7th
    許旭平,謝美娟,甘海燕,梁榮良,韓爾康,楊學(xué)習,吳英松. 基于高通量測序技術(shù)無(wú)創(chuàng )篩查雙胎染色體非整倍體及胎兒游離DNA濃度分析.分子診斷與治療雜志[J],2016,8(6),375-379.
    Link
    6th
    Mei-Juan Xie, Zhi-kun Liang, et al. Noninvasive Prenatal Testing of Rare Autosomal Aneuploidies by Semiconductor Sequencing.DNA Cell Biol. 2018 Mar;37(3):174-181.
    Link
    5th
    Xu-Ping Xu, Hai-Yan Gan, Fen-Xia Li, Qi Tian, Jun Zhang, Rong-Liang Liang, Ming Li, Xue-Xi Yang , Ying-Song Wu. PLOS ONE 2016,10.A Method to Quantify Cell-Free Fetal DNA Fraction in Maternal Plasma Using Next Generation Sequencing: Its Application in Non-Invasive Prenatal Chromosomal Aneuploidy Detection
    Link
    4th
    Sun K, Jiang P, Wong A I, et al. Size-tagged preferred ends in maternal plasma DNA shed light on the production mechanism and show utility in noninvasive prenatal testing[J]. Proceedings of the National Academy of Sciences of the United States of America, 2018, 115(22).
    Link
    3th
    Chan KCA, et al. (2016) Second generation noninvasive fetal genome analysis reveals de novo mutations, single-base parental inheritance, and preferred DNA ends. Proc Natl Acad Sci USA 113:E8159–E8168.
    Link
    2th
    Lo YMD, et al. (2010) Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus. Sci Transl Med 2:61ra91.
    Link
    1th
    van Opstal D, et al. (2018) Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: Results of the TRIDENT study. Genet Med 20:480–485.
    Link

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