These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

187 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 Sep; 310(3):1779-1785. PubMed ID: 38625542
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Diagnostic and prognostic role of soft ultrasound markers in prenatal detection and assessment of foetal abnormalities.
    Moradi B; Bahrami A; Vafaei SM; Sharifpour S; Shariatinia F; Rezvanimehr A; Rashidi-Nezhad A; Fathi M; Yaghoobpoor S; Ghorani H
    Prz Menopauzalny; 2024 Jun; 23(2):94-108. PubMed ID: 39391522
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. [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]  

  • 7. 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]  

  • 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. 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]  

  • 12. 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]  

  • 13. [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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. [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]  

  • 18. 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]  

  • 19. 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]  

  • 20. Comparison of Efficiencies of Non-invasive Prenatal Testing, Karyotyping, and Chromosomal Micro-Array for Diagnosing Fetal Chromosomal Anomalies in the Second and Third Trimesters.
    Zhu Y; Shan Q; Zheng J; Cai Q; Yang H; Zhang J; Du X; Jin F
    Front Genet; 2019; 10():69. PubMed ID: 30915098
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.