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Journal Abstract Search

697 related items for PubMed ID: 23553438

  • 1. 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; 33(6):602-8. PubMed ID: 23553438
    [Abstract] [Full Text] [Related]

  • 2. 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; 43(3):254-64. PubMed ID: 24339153
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  • 3. Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing.
    Liang D, Lv W, Wang H, Xu L, Liu J, Li H, Hu L, Peng Y, Wu L.
    Prenat Diagn; 2013 May; 33(5):409-15. PubMed ID: 23299662
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  • 7. 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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  • 9. [Non invasive prenatal test (NIPT) in maternal blood by parallel massive sequencing. Initial experience in Mexican women and literature review].
    Hernández-Gómez M, Ramirez-Arroyo E, Meléndez-Hernández R, Garduño-Zaraza LM, Mayén-Molina DG.
    Ginecol Obstet Mex; 2015 May 11; 83(5):277-88. PubMed ID: 26233973
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  • 10. Discordant results between fetal karyotyping and non-invasive prenatal testing by maternal plasma sequencing in a case of uniparental disomy 21 due to trisomic rescue.
    Pan M, Li FT, Li Y, Jiang FM, Li DZ, Lau TK, Liao C.
    Prenat Diagn; 2013 Jun 11; 33(6):598-601. PubMed ID: 23533085
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  • 11. 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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  • 12. Clinical experience of noninvasive prenatal testing with cell-free DNA for fetal trisomies 21, 18, and 13, in a general screening population.
    Fairbrother G, Johnson S, Musci TJ, Song K.
    Prenat Diagn; 2013 Jun 10; 33(6):580-3. PubMed ID: 23494956
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  • 14. Non-invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146,958 pregnancies.
    Zhang H, Gao Y, Jiang F, Fu M, Yuan Y, Guo Y, Zhu Z, Lin M, Liu Q, Tian Z, Zhang H, Chen F, Lau TK, Zhao L, Yi X, Yin Y, Wang W.
    Ultrasound Obstet Gynecol; 2015 May 10; 45(5):530-8. PubMed ID: 25598039
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  • 15. Open source non-invasive prenatal testing platform and its performance in a public health laboratory.
    Johansen P, Richter SR, Balslev-Harder M, Miltoft CB, Tabor A, Duno M, Kjaergaard S.
    Prenat Diagn; 2016 Jun 10; 36(6):530-6. PubMed ID: 27027563
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  • 16. Validation of targeted sequencing of single-nucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y.
    Nicolaides KH, Syngelaki A, Gil M, Atanasova V, Markova D.
    Prenat Diagn; 2013 Jun 10; 33(6):575-9. PubMed ID: 23613152
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  • 17. Noninvasive prenatal screening for fetal common sex chromosome aneuploidies from maternal blood.
    Zhang B, Lu BY, Yu B, Zheng FX, Zhou Q, Chen YP, Zhang XQ.
    J Int Med Res; 2017 Apr 10; 45(2):621-630. PubMed ID: 28357876
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  • 19. Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.
    Bianchi DW, Platt LD, Goldberg JD, Abuhamad AZ, Sehnert AJ, Rava RP, MatErnal BLood IS Source to Accurately diagnose fetal aneuploidy (MELISSA) Study Group.
    Obstet Gynecol; 2012 May 10; 119(5):890-901. PubMed ID: 22362253
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  • 20. Maternal Plasma DNA and RNA Sequencing for Prenatal Testing.
    Tamminga S, van Maarle M, Henneman L, Oudejans CB, Cornel MC, Sistermans EA.
    Adv Clin Chem; 2016 May 10; 74():63-102. PubMed ID: 27117661
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