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Journal Abstract Search

327 related items for PubMed ID: 31439719

  • 1. Long-read sequencing and haplotype linkage analysis enabled preimplantation genetic testing for patients carrying pathogenic inversions.
    Zhang S, Liang F, Lei C, Wu J, Fu J, Yang Q, Luo X, Yu G, Wang D, Zhang Y, Lu D, Sun X, Liang Y, Xu C.
    J Med Genet; 2019 Nov; 56(11):741-749. PubMed ID: 31439719
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  • 3. Identifying Balanced Chromosomal Translocations in Human Embryos by Oxford Nanopore Sequencing and Breakpoints Region Analysis.
    Pei Z, Deng K, Lei C, Du D, Yu G, Sun X, Xu C, Zhang S.
    Front Genet; 2021 Nov; 12():810900. PubMed ID: 35116057
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  • 7. Preclinical workup using long-read amplicon sequencing provides families with de novo pathogenic variants access to universal preimplantation genetic testing.
    Tsuiko O, El Ayeb Y, Jatsenko T, Allemeersch J, Melotte C, Ding J, Debrock S, Peeraer K, Vanhie A, De Leener A, Pirard C, Kluyskens C, Denayer E, Legius E, Vermeesch JR, Brems H, Dimitriadou E.
    Hum Reprod; 2023 Mar 01; 38(3):511-519. PubMed ID: 36625546
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  • 10. Haplotyping by linked-read sequencing (HLRS) of the genetic disease carriers for preimplantation genetic testing without a proband or relatives.
    Li Q, Mao Y, Li S, Du H, He W, He J, Kong L, Zhang J, Liang B, Liu J.
    BMC Med Genomics; 2020 Aug 20; 13(1):117. PubMed ID: 32819358
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  • 11. [Application of single-sperm sequencing in resolving the carrier status of preimplantation genetic testing for chromosomal structural rearrangements in Robertsonian translocations].
    Liao BQ, Lai LD, Liu RT, Zhang Q, Lian WC, Xie WM.
    Zhonghua Nan Ke Xue; 2024 Jun 20; 30(6):499-506. PubMed ID: 39212358
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  • 14. Multi-centre evaluation of a comprehensive preimplantation genetic test through haplotyping-by-sequencing.
    Masset H, Zamani Esteki M, Dimitriadou E, Dreesen J, Debrock S, Derhaag J, Derks K, Destouni A, Drüsedau M, Meekels J, Melotte C, Peeraer K, Tšuiko O, van Uum C, Allemeersch J, Devogelaere B, François KO, Happe S, Lorson D, Richards RL, Theuns J, Brunner H, de Die-Smulders C, Voet T, Paulussen A, Coonen E, Vermeesch JR.
    Hum Reprod; 2019 Aug 01; 34(8):1608-1619. PubMed ID: 31348829
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  • 16. The establishment and application of preimplantation genetic haplotyping in embryo diagnosis for reciprocal and Robertsonian translocation carriers.
    Zhang S, Lei C, Wu J, Zhou J, Sun H, Fu J, Sun Y, Sun X, Lu D, Zhang Y.
    BMC Med Genomics; 2017 Oct 17; 10(1):60. PubMed ID: 29041973
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  • 17. Long-read sequencing on the SMRT platform enables efficient haplotype linkage analysis in preimplantation genetic testing for β-thalassemia.
    Wu H, Chen D, Zhao Q, Shen X, Liao Y, Li P, Chiu PCN, Zhou C.
    J Assist Reprod Genet; 2022 Mar 17; 39(3):739-746. PubMed ID: 35141813
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  • 20. Establishment of linkage phase, using Oxford Nanopore Technologies, for preimplantation genetic testing of Coffin-Lowry syndrome with a de novo RPS6KA3 mutation.
    Wen X, Du J, Li Z, Liu N, Huo J, Li J, Ke W, Wu J, Fang X, Lin X.
    Front Genet; 2023 Mar 17; 14():1169868. PubMed ID: 37779904
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