179 related articles for article (PubMed ID: 38196919)
1. Comparison of Chromosomal Microarray Analysis and Noninvasive Prenatal Testing in Pregnant Women with Fetal Ultrasonic Soft Markers.
Hu X; Hu Y; Wang H; Yu C; Zheng J; Zhang H; Zheng J
Risk Manag Healthc Policy; 2024; 17():29-40. PubMed ID: 38196919
[TBL] [Abstract][Full Text] [Related]
2. Selection of prenatal screening with nuchal translucency > 95th centile and below 99th centile: a 4-year observational study with real-world data.
Zhang B; Zhang LX; Yi J; Wang CH; Zhao Y
Arch Gynecol Obstet; 2024 Apr; ():. PubMed ID: 38625542
[TBL] [Abstract][Full Text] [Related]
3. Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype.
Su L; Huang H; An G; Cai M; Wu X; Li Y; Xie X; Lin Y; Wang M; Xu L
Mol Genet Genomic Med; 2019 Aug; 7(8):e811. PubMed ID: 31209990
[TBL] [Abstract][Full Text] [Related]
4. Performance of Chromosomal Microarray Analysis for Detection of Copy Number Variations in Fetal Echogenic Bowel.
Fan X; Huang H; Lin X; Xue H; Cai M; Lin N; Xu L
Risk Manag Healthc Policy; 2021; 14():1431-1438. PubMed ID: 33859509
[TBL] [Abstract][Full Text] [Related]
5. [Application of chromosomal microarray analysis in prenatal diagnosis of pregnant women with advanced age].
Yang S; Zhao Y; Tang X; Wang Z; Liu D; Zhang J; Gu Y; Wang L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Feb; 38(2):101-107. PubMed ID: 33565058
[TBL] [Abstract][Full Text] [Related]
6. Nuchal translucency of 3.0-3.4 mm an indication for NIPT or microarray? Cohort analysis and literature review.
Petersen OB; Smith E; Van Opstal D; Polak M; Knapen MFCM; Diderich KEM; Bilardo CM; Arends LR; Vogel I; Srebniak MI
Acta Obstet Gynecol Scand; 2020 Jun; 99(6):765-774. PubMed ID: 32306377
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Chromosomal microarray analysis versus noninvasive prenatal testing in fetuses with increased nuchal translucency.
Wang C; Tang J; Tong K; Huang D; Tu H; Zhu J
J Hum Genet; 2022 Sep; 67(9):533-539. PubMed ID: 35578003
[TBL] [Abstract][Full Text] [Related]
9. Evaluation of the clinical utility of extended non-invasive prenatal testing in the detection of chromosomal aneuploidy and microdeletion/microduplication.
Tian W; Yuan Y; Yuan E; Zhang L; Liu L; Li Y; Guo J; Cui X; Li P; Cui S
Eur J Med Res; 2023 Aug; 28(1):304. PubMed ID: 37644576
[TBL] [Abstract][Full Text] [Related]
10. Clinical utility of non-invasive prenatal testing in pregnancies with ultrasound anomalies.
Beulen L; Faas BHW; Feenstra I; van Vugt JMG; Bekker MN
Ultrasound Obstet Gynecol; 2017 Jun; 49(6):721-728. PubMed ID: 27515011
[TBL] [Abstract][Full Text] [Related]
11. Expanding the application of non-invasive prenatal testing in the detection of foetal chromosomal copy number variations.
Wang C; Tang J; Tong K; Huang D; Tu H; Li Q; Zhu J
BMC Med Genomics; 2021 Dec; 14(1):292. PubMed ID: 34895207
[TBL] [Abstract][Full Text] [Related]
12. Application of expanded noninvasive prenatal test in prenatal diagnosis of fetuses with increased nuchal translucency.
Xie X; Zhou H; Zhao Q; Lu Y; Meng Y
J Matern Fetal Neonatal Med; 2022 Dec; 35(25):6213-6218. PubMed ID: 34649482
[TBL] [Abstract][Full Text] [Related]
13. Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal Translucency.
Cicatiello R; Pignataro P; Izzo A; Mollo N; Pezone L; Maruotti GM; Sarno L; Sglavo G; Conti A; Genesio R; Nitsch L
Med Sci (Basel); 2019 Feb; 7(3):. PubMed ID: 30818867
[TBL] [Abstract][Full Text] [Related]
14. [Application of high-throughput sequencing technology for the detection of fetal copy number variations].
Jiang N; Zhang Y; Song L; Yu D
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jul; 37(7):779-784. PubMed ID: 32619264
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Should chromosomal microarray be offered to fetuses with ultrasonographic soft markers in second trimester: A prospective cohort study and meta-analysis.
Li S; Han X; Ye M; Chen S; Shen Y; Niu J; Wang Y; Xu C
Prenat Diagn; 2020 Dec; 40(12):1569-1577. PubMed ID: 32812229
[TBL] [Abstract][Full Text] [Related]
17. Performance of expanded non-invasive prenatal testing for fetal aneuploidies and copy number variations: A prospective study from a single center in Jiangxi province, China.
Zou Y; Feng C; Qin J; Wang X; Huang T; Yang Y; Xie K; Yuan H; Huang S; Yang B; Lu W; Liu Y
Front Genet; 2022; 13():1073851. PubMed ID: 36712884
[TBL] [Abstract][Full Text] [Related]
18. [Report content and prenatal diagnosis of non-invasive prenatal testing for sex chromosome aneuploidy].
Zhou CX; He LL; Zhu XY; Li ZX; Duan HL; Liu W; Gu LL; Li J
Zhonghua Fu Chan Ke Za Zhi; 2023 Oct; 58(10):766-773. PubMed ID: 37849257
[No Abstract] [Full Text] [Related]
19. Prenatal diagnosis of ultrasound soft markers in a single medical center of mainland China.
Zhou Y; Wu S; Han J; Zhen L; Yang X; Li R; Zhang Y; Jing X; Li F; Liu H
Mol Cytogenet; 2023 Feb; 16(1):3. PubMed ID: 36765363
[TBL] [Abstract][Full Text] [Related]
20. Detection of fetal copy number variants by non-invasive prenatal testing for common aneuploidies.
Li R; Wan J; Zhang Y; Fu F; Ou Y; Jing X; Li J; Li D; Liao C
Ultrasound Obstet Gynecol; 2016 Jan; 47(1):53-7. PubMed ID: 26033469
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
