2754 related articles for article (PubMed ID: 29032050)
21. Massively Parallel Sequencing (MPS) of Cell-Free Fetal DNA (cffDNA) for Trisomies 21, 18, and 13 in Twin Pregnancies.
Du E; Feng C; Cao Y; Yao Y; Lu J; Zhang Y
Twin Res Hum Genet; 2017 Jun; 20(3):242-249. PubMed ID: 28485265
[TBL] [Abstract][Full Text] [Related]
22. Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing.
Dar P; Curnow KJ; Gross SJ; Hall MP; Stosic M; Demko Z; Zimmermann B; Hill M; Sigurjonsson S; Ryan A; Banjevic M; Kolacki PL; Koch SW; Strom CM; Rabinowitz M; Benn P
Am J Obstet Gynecol; 2014 Nov; 211(5):527.e1-527.e17. PubMed ID: 25111587
[TBL] [Abstract][Full Text] [Related]
23. Cytogenetic outcomes following a failed cell-free DNA screen: a population-based retrospective cohort study of 35,146 singleton pregnancies.
Bellai-Dussault K; Meng L; Howley H; Reszel J; Huang T; Lanes A; Walker MC; Okun N; Dougan SD; Armour CM
Am J Obstet Gynecol; 2023 Aug; 229(2):168.e1-168.e8. PubMed ID: 36627072
[TBL] [Abstract][Full Text] [Related]
24. Prenatal diagnosis of fetuses with increased nuchal translucency using an approach based on quantitative fluorescent polymerase chain reaction and genomic microarray.
Pan M; Han J; Zhen L; Yang X; Li R; Liao C; Li DZ
Eur J Obstet Gynecol Reprod Biol; 2016 Feb; 197():164-7. PubMed ID: 26771907
[TBL] [Abstract][Full Text] [Related]
25. [Prenatal diagnosis and outcome of pregnancy for women with high risks by screening of fetal free DNA from peripheral blood samples].
Li Z; Duan H; Liu W; Zhu R; Li J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Jan; 41(1):1-7. PubMed ID: 38171551
[TBL] [Abstract][Full Text] [Related]
26. Noninvasive Prenatal Testing for Trisomies 21, 18, and 13, Sex Chromosome Aneuploidies, and Microdeletions: A Health Technology Assessment.
Health Quality Ontario
Ont Health Technol Assess Ser; 2019; 19(4):1-166. PubMed ID: 30847010
[TBL] [Abstract][Full Text] [Related]
27. Women should decide which conditions matter.
Norton ME; Kuppermann M
Am J Obstet Gynecol; 2016 Nov; 215(5):583-587.e1. PubMed ID: 27793311
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. [Application of non-invasive prenatal testing for the screening of fetal chromosomal abnormalities in 12 085 cases].
Wang L; Zhou C; Hu Y; Jin Y; Liu X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Oct; 37(10):1069-1073. PubMed ID: 32924103
[TBL] [Abstract][Full Text] [Related]
30. Replacing the combined test by cell-free DNA testing in screening for trisomies 21, 18 and 13: impact on the diagnosis of other chromosomal abnormalities.
Syngelaki A; Pergament E; Homfray T; Akolekar R; Nicolaides KH
Fetal Diagn Ther; 2014; 35(3):174-84. PubMed ID: 24525399
[TBL] [Abstract][Full Text] [Related]
31. Clinical Validation of Non-Invasive Prenatal Testing for Fetal Common Aneuploidies in 1,055 Korean Pregnant Women: a Single Center Experience.
Lee DE; Kim H; Park J; Yun T; Park DY; Kim M; Ryu HM
J Korean Med Sci; 2019 Jun; 34(24):e172. PubMed ID: 31222985
[TBL] [Abstract][Full Text] [Related]
32. Noninvasive prenatal testing (NIPT) detects variant of Turner syndrome not detectable by fluorescent
Eswarachari V; Kadam P; Movva S; Lingaiah S; Akther RM; Kidangan FX; Gowda KC; Golakoti RRK; Lall M; Mahajan S; Saviour P; Puri R; Verma IC; Vedam RL
J Matern Fetal Neonatal Med; 2019 Dec; 32(24):4177-4180. PubMed ID: 29793366
[No Abstract] [Full Text] [Related]
33. Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes.
Liang D; Cram DS; Tan H; Linpeng S; Liu Y; Sun H; Zhang Y; Tian F; Zhu H; Xu M; Wang H; Yu F; Wu L
Genet Med; 2019 Sep; 21(9):1998-2006. PubMed ID: 30828085
[TBL] [Abstract][Full Text] [Related]
34. [Clinical significance of non-invasive prenatal testing in preventing birth defects].
Zhang W; Li S; Tang P; Wang J; Gu S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Oct; 37(10):1061-1064. PubMed ID: 32924101
[TBL] [Abstract][Full Text] [Related]
35. Relationships among maternal monosomy X mosaicism, maternal trisomy, and discordant sex chromosome aneuploidies.
Tang X; Du Y; Chen M; Zhang Y; Wang Z; Zhang F; Tan J; Yin T; Wang L
Clin Chim Acta; 2024 Feb; 554():117770. PubMed ID: 38199578
[TBL] [Abstract][Full Text] [Related]
36. Performance of prenatal cfDNA screening for sex chromosomes.
Martin K; Dar P; MacPherson C; Egbert M; Demko Z; Parmar S; Hashimoto K; Haeri S; Malone F; Wapner RJ; Roman AS; Khalil A; Faro R; Madankumar R; Strong N; Silver RM; Vohra N; Hyett J; Rabinowitz M; Kao C; Hakonarson H; Jacobsson B; Norton ME
Genet Med; 2023 Aug; 25(8):100879. PubMed ID: 37154148
[TBL] [Abstract][Full Text] [Related]
37. [Result of prenatal diagnosis for 151 high-risk women by noninvasive prenatal screening based on high-throughput sequencing].
Jia Y; Zhang Y; Hao W; Shi D; Meng J; Zhao H; Lian Y; Xie L; Wang X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct; 34(5):759-763. PubMed ID: 28981949
[TBL] [Abstract][Full Text] [Related]
38. Non-invasive prenatal testing for detection of trisomy 13, 18, 21 and sex chromosome aneuploidies in 8594 cases.
Zheng Y; Wan S; Dang Y; Song T; Chen B; Zhang J
Ginekol Pol; 2019; 90(5):270-273. PubMed ID: 31165466
[TBL] [Abstract][Full Text] [Related]
39. 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; 45(5):530-8. PubMed ID: 25598039
[TBL] [Abstract][Full Text] [Related]
40. Clinical performance of non-invasive prenatal served as a first-tier screening test for trisomy 21, 18, 13 and sex chromosome aneuploidy in a pilot city in China.
Liu Y; Liu H; He Y; Xu W; Ma Q; He Y; Lei W; Chen G; He Z; Huang J; Liu J; Liu Y; Huang Q; Yu F
Hum Genomics; 2020 Jun; 14(1):21. PubMed ID: 32503639
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]