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Journal Abstract Search

1121 related items for PubMed ID: 26260800

  • 1. Discordant circulating fetal DNA and subsequent cytogenetics reveal false negative, placental mosaic, and fetal mosaic cfDNA genotypes.
    Lebo RV, Novak RW, Wolfe K, Michelson M, Robinson H, Mancuso MS.
    J Transl Med; 2015 Aug 11; 13():260. PubMed ID: 26260800
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  • 2. A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21.
    Li J, Xie M, Wang F, Ma J, Li J, Chen C, Li Z, Wang J, Zhang Y, Li Y.
    Mol Genet Genomic Med; 2020 Aug 11; 8(8):e1279. PubMed ID: 32463164
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  • 3. Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center.
    Lau TK, Cheung SW, Lo PS, Pursley AN, Chan MK, Jiang F, Zhang H, Wang W, Jong LF, Yuen OK, Chan HY, Chan WS, Choy KW.
    Ultrasound Obstet Gynecol; 2014 Mar 11; 43(3):254-64. PubMed ID: 24339153
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  • 7. [Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester].
    Zhang YP, Wu JP, Li XT, Lei CX, Xu JZ, Yin M.
    Zhonghua Fu Chan Ke Za Zhi; 2011 Sep 11; 46(9):644-8. PubMed ID: 22176986
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  • 8. Secondary findings from non-invasive prenatal testing for common fetal aneuploidies by whole genome sequencing as a clinical service.
    Lau TK, Jiang FM, Stevenson RJ, Lo TK, Chan LW, Chan MK, Lo PS, Wang W, Zhang HY, Chen F, Choy KW.
    Prenat Diagn; 2013 Jun 11; 33(6):602-8. PubMed ID: 23553438
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  • 9. [Genetic study of a trisomy 13 fetus with a false-negative karyotype by chorionic villi analysis].
    Shi S, Zha Q, Shi Z, Li R.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Aug 10; 37(8):839-842. PubMed ID: 32761590
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  • 12. Cytogenetic confirmation of a positive NIPT result: evidence-based choice between chorionic villus sampling and amniocentesis depending on chromosome aberration.
    Van Opstal D, Srebniak MI.
    Expert Rev Mol Diagn; 2016 Aug 10; 16(5):513-20. PubMed ID: 26864482
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  • 13. Accuracy of cytogenetic findings on chorionic villus sampling (CVS)--diagnostic consequences of CVS mosaicism and non-mosaic discrepancy in centres contributing to EUCROMIC 1986-1992.
    Hahnemann JM, Vejerslev LO.
    Prenat Diagn; 1997 Sep 10; 17(9):801-20. PubMed ID: 9316125
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  • 14. Confined placental origin of the circulating cell free fetal DNA revealed by a discordant non-invasive prenatal test result in a trisomy 18 pregnancy.
    Mao J, Wang T, Wang BJ, Liu YH, Li H, Zhang J, Cram D, Chen Y.
    Clin Chim Acta; 2014 Jun 10; 433():190-3. PubMed ID: 24667696
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  • 17. Implications of fetoplacental mosaicism on cell-free DNA testing for sex chromosome aneuploidies.
    Grati FR, Bajaj K, Zanatta V, Malvestiti F, Malvestiti B, Marcato L, Grimi B, Maggi F, Simoni G, Gross SJ, Ferreira J.
    Prenat Diagn; 2017 Oct 10; 37(10):1017-1027. PubMed ID: 28801976
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  • 18. A gradual change of chromosome mosaicism from placenta to fetus leading to T18 false negative result by NIPS.
    Wang Z, Tang X, Yang S, Yin T, Zhao Y, Zheng A, Zhang R, Gu Y, Wang L.
    Clin Chim Acta; 2019 Aug 10; 495():263-268. PubMed ID: 30998911
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  • 19. Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory.
    Petersen AK, Cheung SW, Smith JL, Bi W, Ward PA, Peacock S, Braxton A, Van Den Veyver IB, Breman AM.
    Am J Obstet Gynecol; 2017 Dec 10; 217(6):691.e1-691.e6. PubMed ID: 29032050
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