236 related articles for article (PubMed ID: 36819517)
41. [Is it necessary to choose NIPT-plus for pregnant women who opt for non-invasive prenatal testing? A study of 50 cases].
Dai P; Zhao G; Gao S; Chen S; Zhang F; Guo W; Kong X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Sep; 38(9):895-899. PubMed ID: 34487540
[TBL] [Abstract][Full Text] [Related]
42. Whole genome non-invasive prenatal testing in prenatal screening algorithm: clinical experience from 12,700 pregnancies.
Baranova EE; Sagaydak OV; Galaktionova AM; Kuznetsova ES; Kaplanova MT; Makarova MV; Belenikin MS; Olenev AS; Songolova EN
BMC Pregnancy Childbirth; 2022 Aug; 22(1):633. PubMed ID: 35945516
[TBL] [Abstract][Full Text] [Related]
43. Noninvasive prenatal testing, ultrasonographic findings and poor prenatal diagnosis rates for twin pregnancies: a retrospective study.
Yuan X; Wang W; Dai L; Yong W; Pei C; Li J; Wu L
BMC Pregnancy Childbirth; 2023 May; 23(1):351. PubMed ID: 37179315
[TBL] [Abstract][Full Text] [Related]
44. Evaluation of the clinical effects of non-invasive prenatal screening for diseases associated with aneuploidy and copy number variation.
Zhu S; Jia C; Hao S; Zhang Q; He J; Wang X; Lin P; Guo Y; Li Y; Feng X
Mol Genet Genomic Med; 2023 Sep; 11(9):e2200. PubMed ID: 37354111
[TBL] [Abstract][Full Text] [Related]
45. Study on the Clinical Value of Noninvasive Prenatal Testing in Screening the Chromosomal Abnormalities of the Fetus in the Elderly Pregnant Women.
Gu Z; Du M; Xu T; Jin C
Comput Math Methods Med; 2022; 2022():2977128. PubMed ID: 36213582
[TBL] [Abstract][Full Text] [Related]
46. The performance evaluation of NIPT for fetal chromosome microdeletion/microduplication detection: a retrospective analysis of 68,588 Chinese cases.
Shen S; Qi H; Yuan X; Gan J; Chen J; Huang J
Front Genet; 2024; 15():1390539. PubMed ID: 38911296
[TBL] [Abstract][Full Text] [Related]
47. Contingent first-trimester screening for aneuploidies with cell-free DNA in a Danish clinical setting.
Miltoft CB; Rode L; Ekelund CK; Sundberg K; Kjaergaard S; Zingenberg H; Tabor A
Ultrasound Obstet Gynecol; 2018 Apr; 51(4):470-479. PubMed ID: 28640470
[TBL] [Abstract][Full Text] [Related]
48. 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]
49. Expanded noninvasive prenatal testing for fetal aneuploidy and copy number variations and parental willingness for invasive diagnosis in a cohort of 18,516 cases.
Ge Y; Li J; Zhuang J; Zhang J; Huang Y; Tan M; Li W; Chen J; Zhou Y
BMC Med Genomics; 2021 Apr; 14(1):106. PubMed ID: 33853619
[TBL] [Abstract][Full Text] [Related]
50. State-wide utilization and performance of traditional and cell-free DNA-based prenatal testing pathways: the Victorian Perinatal Record Linkage (PeRL) study.
Lindquist A; Hui L; Poulton A; Kluckow E; Hutchinson B; Pertile MD; Bonacquisto L; Gugasyan L; Kulkarni A; Harraway J; Howden A; McCoy R; Da Silva Costa F; Menezes M; Palma-Dias R; Nisbet D; Martin N; Bethune M; Poulakis Z; Halliday J
Ultrasound Obstet Gynecol; 2020 Aug; 56(2):215-224. PubMed ID: 31625225
[TBL] [Abstract][Full Text] [Related]
51. Efficiency of expanded noninvasive prenatal testing in the detection of fetal subchromosomal microdeletion and microduplication in a cohort of 31,256 single pregnancies.
Xue H; Yu A; Lin M; Chen X; Guo Q; Xu L; Huang H
Sci Rep; 2022 Nov; 12(1):19750. PubMed ID: 36396840
[TBL] [Abstract][Full Text] [Related]
52. The Clinical Utility of Non-invasive Prenatal Testing for Pregnant Women With Different Diagnostic Indications.
Zheng J; Lu H; Li M; Guan Y; Yang F; Xu M; Dong J; Zhang Q; An N; Zhou Y
Front Genet; 2020; 11():624. PubMed ID: 32695138
[TBL] [Abstract][Full Text] [Related]
53. The detection efficacy of noninvasive prenatal genetic testing (NIPT) for sex chromosome abnormalities and copy number variation and its differentiation in pregnant women of different ages.
Li Y; Yang X; Zhang Y; Lou H; Wu M; Liu F; Chang W; Zhao X
Heliyon; 2024 Jan; 10(2):e24155. PubMed ID: 38293423
[TBL] [Abstract][Full Text] [Related]
54. Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 42,910 single pregnancies with different clinical features.
Chen Y; Yu Q; Mao X; Lei W; He M; Lu W
Hum Genomics; 2019 Nov; 13(1):60. PubMed ID: 31783780
[TBL] [Abstract][Full Text] [Related]
55. 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]
56. [The value of non-invasive prenatal testing for the identification of numerical and structural chromosomal abnormalities and copy number variations in the fetuses].
Hou S; Zhang H; Li C; Chen D; Yan H; Yang M; Liu Y; Lei D
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Oct; 40(10):1197-1203. PubMed ID: 37730217
[TBL] [Abstract][Full Text] [Related]
57. A study on non-invasive prenatal screening for the detection of aneuploidy.
Chen Y; Yang F; Shang X; Liu S; Li M; Zhong M
Ginekol Pol; 2022; 93(9):716-720. PubMed ID: 35315016
[TBL] [Abstract][Full Text] [Related]
58. [Clinical application and evaluation of health economics for non-invasive prenatal testing of fetuses in Tianjin].
Ma R; Li X; Xu S; Shi Y; Ju D; Li Y; Meng F; Wang X; Du X; Xu N; Zhang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Feb; 40(2):135-142. PubMed ID: 36709929
[TBL] [Abstract][Full Text] [Related]
59. 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]
60. 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
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
