BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

247 related articles for article (PubMed ID: 32632923)

  • 21. Application of chromosome microarray analysis and karyotyping in diagnostic assessment of abnormal Down syndrome screening results.
    Kang H; Wang L; Li X; Gao C; Xie Y; Hu Y
    BMC Pregnancy Childbirth; 2022 Nov; 22(1):813. PubMed ID: 36333674
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 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]  

  • 24. Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
    Petrovski S; Aggarwal V; Giordano JL; Stosic M; Wou K; Bier L; Spiegel E; Brennan K; Stong N; Jobanputra V; Ren Z; Zhu X; Mebane C; Nahum O; Wang Q; Kamalakaran S; Malone C; Anyane-Yeboa K; Miller R; Levy B; Goldstein DB; Wapner RJ
    Lancet; 2019 Feb; 393(10173):758-767. PubMed ID: 30712878
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Application of single nucleotide polymorphism array in prenatal diagnosis for fetuses with abnormal ultrasound findings].
    Guo YL; Wang L; Xue SW; Qu SZ; Yang J; Xu H; Bai ZX; Liu N; Kong XD
    Zhonghua Fu Chan Ke Za Zhi; 2018 Jul; 53(7):464-470. PubMed ID: 30078256
    [No Abstract]   [Full Text] [Related]  

  • 26. Prenatal chromosomal microarray testing of fetuses with ultrasound structural anomalies: A prospective cohort study of over 1000 consecutive cases.
    Chong HP; Hamilton S; Mone F; Cheung KW; Togneri FS; Morris RK; Quinlan-Jones E; Williams D; Allen S; McMullan DJ; Kilby MD
    Prenat Diagn; 2019 Nov; 39(12):1064-1069. PubMed ID: 31393021
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Added value of chromosomal microarray analysis over karyotyping in early pregnancy loss: systematic review and meta-analysis.
    Pauta M; Grande M; Rodriguez-Revenga L; Kolomietz E; Borrell A
    Ultrasound Obstet Gynecol; 2018 Apr; 51(4):453-462. PubMed ID: 29055063
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [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]  

  • 29. Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities.
    Fiorentino F; Napoletano S; Caiazzo F; Sessa M; Bono S; Spizzichino L; Gordon A; Nuccitelli A; Rizzo G; Baldi M
    Eur J Hum Genet; 2013 Jul; 21(7):725-30. PubMed ID: 23211699
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Detection of submicroscopic chromosomal aberrations by chromosomal microarray analysis for the prenatal diagnosis of central nervous system abnormalities.
    Song T; Xu Y; Li Y; Jia L; Zheng J; Dang Y; Wan S; Zheng Y; Zhang J; Yang H
    J Clin Lab Anal; 2020 Oct; 34(10):e23434. PubMed ID: 32677110
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Value of chromosomal microarray analysis for the prenatal diagnosis of pregnancy with high risk signaled by non-invasive prenatal testing].
    Bu X; Zeng L; Li H; Zhou S; Hu L; He J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Jun; 38(6):541-544. PubMed ID: 34096021
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The yield of chromosomal microarray analysis among pregnancies terminated due to fetal malformations.
    Pasternak Y; Daykan Y; Tenne T; Reinstein E; Miller N; Shechter-Maor G; Maya I; Biron-Shental T; Sukenik Halevy R
    J Matern Fetal Neonatal Med; 2022 Jan; 35(2):336-340. PubMed ID: 31973614
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis.
    Wang H; Dong Z; Zhang R; Chau MHK; Yang Z; Tsang KYC; Wong HK; Gui B; Meng Z; Xiao K; Zhu X; Wang Y; Chen S; Leung TY; Cheung SW; Kwok YK; Morton CC; Zhu Y; Choy KW
    Genet Med; 2020 Mar; 22(3):500-510. PubMed ID: 31447483
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Dilemmas in genetic counseling for low-penetrance neuro-susceptibility loci detected on prenatal chromosomal microarray analysis.
    Brabbing-Goldstein D; Reches A; Svirsky R; Bar-Shira A; Yaron Y
    Am J Obstet Gynecol; 2018 Feb; 218(2):247.e1-247.e12. PubMed ID: 29146387
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosis.
    Chau MHK; Cao Y; Kwok YKY; Chan S; Chan YM; Wang H; Yang Z; Wong HK; Leung TY; Choy KW
    Am J Obstet Gynecol; 2019 Nov; 221(5):493.e1-493.e11. PubMed ID: 31207233
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [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]  

  • 37. Should prenatal chromosomal microarray analysis be offered for isolated fetal growth restriction? A French multicenter study.
    Monier I; Receveur A; Houfflin-Debarge V; Goua V; Castaigne V; Jouannic JM; Mousty E; Saliou AH; Bouchghoul H; Rousseau T; Valat AS; Groussolles M; Fuchs F; Benoist G; Degre S; Massardier J; Tsatsaris V; Kleinfinger P; Zeitlin J; Benachi A;
    Am J Obstet Gynecol; 2021 Dec; 225(6):676.e1-676.e15. PubMed ID: 34058167
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Microarrays in prenatal diagnosis.
    Oneda B; Rauch A
    Best Pract Res Clin Obstet Gynaecol; 2017 Jul; 42():53-63. PubMed ID: 28215395
    [TBL] [Abstract][Full Text] [Related]  

  • 39. What have we learned from 691 prenatal chromosomal microarrays for ventricular septal defects?
    Maya I; Singer A; Yonath H; Reches A; Rienstein S; Zeligson S; Ben Shachar S; Sagi-Dain L
    Acta Obstet Gynecol Scand; 2020 Jun; 99(6):757-764. PubMed ID: 31424084
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Universal chromosomal microarray analysis reveals high proportion of copy-number variants in low-risk pregnancies.
    Stern S; Hacohen N; Meiner V; Yagel S; Zenvirt S; Shkedi-Rafid S; Macarov M; Valsky DV; Porat S; Yanai N; Frumkin A; Daum H
    Ultrasound Obstet Gynecol; 2021 May; 57(5):813-820. PubMed ID: 32202684
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.