BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 31691324)

  • 21. Clinical experience from Thailand: noninvasive prenatal testing as screening tests for trisomies 21, 18 and 13 in 4736 pregnancies.
    Manotaya S; Xu H; Uerpairojkit B; Chen F; Charoenvidhya D; Liu H; Petcharaburanin N; Liu Y; Tang S; Wang X; Dansakul S; Thomsopa T; Gao Y; Zhang H; Xu H; Jiang H
    Prenat Diagn; 2016 Mar; 36(3):224-31. PubMed ID: 26748603
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Performance of Momguard, a new non-invasive prenatal testing protocol developed in Korea.
    Lee MY; Cho DY; Won HS; Hwang AR; Jeong B; Kim J; Oh M
    Obstet Gynecol Sci; 2015 Sep; 58(5):340-5. PubMed ID: 26430657
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [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; 83(5):277-88. PubMed ID: 26233973
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Massively parallel sequencing of maternal plasma DNA in 113 cases of fetal nuchal cystic hygroma.
    Bianchi DW; Prosen T; Platt LD; Goldberg JD; Abuhamad AZ; Rava RP; Sehnert AJ;
    Obstet Gynecol; 2013 May; 121(5):1057-1062. PubMed ID: 23635743
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Establishing and validating noninvasive prenatal testing procedure for fetal aneuploidies in Vietnam.
    Phan MD; Nguyen TV; Trinh HNT; Vo BT; Nguyen TM; Nguyen NH; Nguyen TTQ; Do TTT; Hoang TTD; Truong KD; Giang H; Nguyen HN
    J Matern Fetal Neonatal Med; 2019 Dec; 32(23):4009-4015. PubMed ID: 29865915
    [No Abstract]   [Full Text] [Related]  

  • 26. A retrospective analysis the clinic data and follow-up of non-invasive prenatal test in detection of fetal chromosomal aneuploidy in more than 40,000 cases in a single prenatal diagnosis center.
    Luo Y; Hu H; Jiang L; Ma Y; Zhang R; Xu J; Pan Y; Long Y; Yao H; Liang Z
    Eur J Med Genet; 2020 Sep; 63(9):104001. PubMed ID: 32622960
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Noninvasive Prenatal Screening for Common Fetal Aneuploidies Using Single-Molecule Sequencing.
    Qian Y; Liu Y; Yan K; Xu Y; Sun Y; Gao X; Chen N; Jin P; Zeng L; Sun L; Yan Q; Dong M
    Lab Invest; 2023 Apr; 103(4):100043. PubMed ID: 36870287
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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; 433():190-3. PubMed ID: 24667696
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Association of maternal risk factors with fetal aneuploidy and the accuracy of prenatal aneuploidy screening: a correlation analysis based on 12,186 karyotype reports.
    Wei L; Zhang J; Shi N; Luo C; Bo L; Lu X; Gao S; Mao C
    BMC Pregnancy Childbirth; 2023 Mar; 23(1):136. PubMed ID: 36864406
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Prospective head-to-head comparison of accuracy of two sequencing platforms for screening for fetal aneuploidy by cell-free DNA: the PEGASUS study.
    Rousseau F; Langlois S; Johnson JA; Gekas J; Bujold E; Audibert F; Walker M; Giroux S; Caron A; Clément V; Blais J; MacLeod T; Moore R; Gauthier J; Jouan L; Laporte A; Diallo O; Parker J; Swanson L; Zhao Y; Labelle Y; Giguère Y; Forest JC; Little J; Karsan A; Rouleau G
    Eur J Hum Genet; 2019 Nov; 27(11):1701-1715. PubMed ID: 31231136
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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; 36(6):530-6. PubMed ID: 27027563
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Noninvasive prenatal testing in routine clinical practice--an audit of NIPT and combined first-trimester screening in an unselected Australian population.
    McLennan A; Palma-Dias R; da Silva Costa F; Meagher S; Nisbet DL; Scott F
    Aust N Z J Obstet Gynaecol; 2016 Feb; 56(1):22-8. PubMed ID: 26817523
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.
    Bianchi DW; Platt LD; Goldberg JD; Abuhamad AZ; Sehnert AJ; Rava RP;
    Obstet Gynecol; 2012 May; 119(5):890-901. PubMed ID: 22362253
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low-pass whole-genome sequencing.
    Yu D; Zhang K; Han M; Pan W; Chen Y; Wang Y; Jiao H; Duan L; Zhu Q; Song X; Hong Y; Chen C; Wang J; Hui F; Huang L; Chen C; Du Y
    Mol Genet Genomic Med; 2019 Jun; 7(6):e674. PubMed ID: 31004415
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Prenatal screening for fetal aneuploidies with cell-free DNA in the general pregnancy population: a cost-effectiveness analysis.
    Fairbrother G; Burigo J; Sharon T; Song K
    J Matern Fetal Neonatal Med; 2016; 29(7):1160-4. PubMed ID: 26000626
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Noninvasive Prenatal Testing of Rare Autosomal Aneuploidies by Semiconductor Sequencing.
    Xie MJ; Liang ZK; He D; Xu WW; Wu YS; Yang XX; Li M
    DNA Cell Biol; 2018 Mar; 37(3):174-181. PubMed ID: 29381401
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variants.
    Lefkowitz RB; Tynan JA; Liu T; Wu Y; Mazloom AR; Almasri E; Hogg G; Angkachatchai V; Zhao C; Grosu DS; McLennan G; Ehrich M
    Am J Obstet Gynecol; 2016 Aug; 215(2):227.e1-227.e16. PubMed ID: 26899906
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Noninvasive Prenatal Testing and Incidental Detection of Occult Maternal Malignancies.
    Bianchi DW; Chudova D; Sehnert AJ; Bhatt S; Murray K; Prosen TL; Garber JE; Wilkins-Haug L; Vora NL; Warsof S; Goldberg J; Ziainia T; Halks-Miller M
    JAMA; 2015 Jul; 314(2):162-9. PubMed ID: 26168314
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations.
    Neveling K; Tjwan Thung D; Beulen L; van Rens-Buijsman W; Gomes I; van den Heuvel S; Mieloo H; Derks-Prinsen I; Kater-Baats E; Faas BH
    Prenat Diagn; 2016 Mar; 36(3):216-23. PubMed ID: 26774010
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Feasibility study of semiconductor sequencing for noninvasive prenatal detection of fetal aneuploidy.
    Yuan Y; Jiang F; Hua S; Du B; Hao Y; Ye L; Liu J; Feng K; Huang X; Yi X; Wang W; Yang L; Mu F; Liu C; Liang Y
    Clin Chem; 2013 May; 59(5):846-9. PubMed ID: 23364181
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.