323 related articles for article (PubMed ID: 34649482)
21. Prenatal screening for and diagnosis of aneuploidy in twin pregnancies.
Audibert F; Gagnon A; ;
J Obstet Gynaecol Can; 2011 Jul; 33(7):754-67. PubMed ID: 21749753
[TBL] [Abstract][Full Text] [Related]
22. [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]
23. [Re-evaluation of indications for prenatal diagnosis of advanced pregnant women under the new screening regime].
Yang Y; Wang Y; Gao J; Wu Y; Sun J; Zhao X; Gao L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Oct; 37(10):1057-1060. PubMed ID: 32924100
[TBL] [Abstract][Full Text] [Related]
24. Reexamining the optimal nuchal translucency cutoff for diagnostic testing in the cell-free DNA and microarray era: results from the Victorian Perinatal Record Linkage study.
Hui L; Pynaker C; Bonacquisto L; Lindquist A; Poulton A; Kluckow E; Hutchinson B; Norris F; Pertile MD; 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
Am J Obstet Gynecol; 2021 Nov; 225(5):527.e1-527.e12. PubMed ID: 33957116
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. [Practice of clinical application of noninvasive prenatal testing based on cell-free fetal DNA].
Duan H; Wang W; Zhang Y; Liu W; Gu L; Li J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Mar; 39(3):264-268. PubMed ID: 35315033
[TBL] [Abstract][Full Text] [Related]
27. Prenatal screening for fetal aneuploidy in singleton pregnancies.
Chitayat D; Langlois S; Douglas Wilson R; ;
J Obstet Gynaecol Can; 2011 Jul; 33(7):736-750. PubMed ID: 21749752
[TBL] [Abstract][Full Text] [Related]
28. Application of non-invasive prenatal testing in screening chromosomal aberrations in pregnancies with different nuchal translucency cutoffs.
Xu Y; Hu S; Chen L; Hao Y; Zhang H; Xu Z; Wu W; Deng L
Mol Cytogenet; 2023 Oct; 16(1):29. PubMed ID: 37898768
[TBL] [Abstract][Full Text] [Related]
29. Clinical application of expanded noninvasive prenatal testing for fetal chromosome abnormalities in a cohort of 39,580 pregnancies.
Chen Y; Lu L; Zhang Y; Wang F; Ni Y; Wang Q; Ying C
Am J Med Genet A; 2022 May; 188(5):1426-1434. PubMed ID: 35107205
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Fetal anatomy scan with integrated nuchal translucency and combination of PAPP-A and fβhCG for prediction of aneuploidy.
Kornanova E; Dugatova M; Vaclavova Z; Borovsky M
Bratisl Lek Listy; 2022; 123(4):299-303. PubMed ID: 35294217
[TBL] [Abstract][Full Text] [Related]
32. Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study.
Egloff M; Hervé B; Quibel T; Jaillard S; Le Bouar G; Uguen K; Saliou AH; Valduga M; Perdriolle E; Coutton C; Coston AL; Coussement A; Anselem O; Missirian C; Bretelle F; Prieur F; Fanget C; Muti C; Jacquemot MC; Beneteau C; Le Vaillant C; Vekemans M; Salomon LJ; Vialard F; Malan V
Ultrasound Obstet Gynecol; 2018 Dec; 52(6):715-721. PubMed ID: 29027723
[TBL] [Abstract][Full Text] [Related]
33. Estimation of Detection Rates of Aneuploidy in High-Risk Pregnancy Using an Approach Based on Nuchal Translucency and Non-Invasive Prenatal Testing: A Cohort Study.
Khalil A; Mahmoodian N; Kulkarni A; Homfray T; Papageorghiou A; Bhide A; Thilaganathan B
Fetal Diagn Ther; 2015; 38(4):254-61. PubMed ID: 25925597
[TBL] [Abstract][Full Text] [Related]
34. Application of chromosomal microarray in fetuses with increased nuchal translucency.
Zhao XR; Gao L; Wu Y; Wang YL
J Matern Fetal Neonatal Med; 2020 May; 33(10):1749-1754. PubMed ID: 30688128
[No Abstract] [Full Text] [Related]
35. [Accidental discovery of copy number variation on chromosome 1 in a fetus with high risk of trisomy 13 suggested by NIPT].
Chang J; Song Y; Qi Q; Hao N; Liu J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Aug; 40(8):922-927. PubMed ID: 37532489
[TBL] [Abstract][Full Text] [Related]
36. [Prospective cohort study of fetal nuchal translucency in first-trimester and pregnancy outcome].
Tang HR; Zhang Y; Ru T; Li J; Yang L; Xu Y; Duan HL; Wang Y; Wang Y; Hu YL; Zhang Y; Zheng MM
Zhonghua Fu Chan Ke Za Zhi; 2020 Feb; 55(2):94-99. PubMed ID: 32146737
[No Abstract] [Full Text] [Related]
37. Array study in fetuses with nuchal translucency above the 95th percentile: a 4-year observational single-centre study.
Coello-Cahuao E; Sánchez-Durán MÁ; Calero I; Higueras MT; García MA; Rodó C; Maiz N; Plaja Rustein A; Castells-Sarret N; Mediano-Vizuete C; Carreras E
Arch Gynecol Obstet; 2023 Jan; 307(1):285-292. PubMed ID: 35486155
[TBL] [Abstract][Full Text] [Related]
38. [Prenatal diagnosis of two fetuses with Xp22.31 microdeletion syndrome indicated by non-invasive prenatal testing].
Wang R; Xi M; Wei Y; Wei L; Zhu W; Liu Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Aug; 40(8):928-932. PubMed ID: 37532490
[TBL] [Abstract][Full Text] [Related]
39. Maternal X chromosome copy number variations are associated with discordant fetal sex chromosome aneuploidies detected by noninvasive prenatal testing.
Wang S; Huang S; Ma L; Liang L; Zhang J; Zhang J; Cram DS
Clin Chim Acta; 2015 Apr; 444():113-6. PubMed ID: 25689220
[TBL] [Abstract][Full Text] [Related]
40. Combined use of karyotyping and copy number variation sequencing technology in prenatal diagnosis.
Zhang S; Xu Y; Lu D; Fu D; Zhao Y
PeerJ; 2022; 10():e14400. PubMed ID: 36523456
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]