BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

247 related articles for article (PubMed ID: 36636555)

  • 21. Prenatal diagnosis of fetuses with absent/hypoplastic nasal bone in second-trimester using chromosomal microarray analysis.
    Chen X; Jiang Y; Zeng S; Zhuang J; Lin N
    Birth Defects Res; 2024 May; 116(5):e2351. PubMed ID: 38766695
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prenatal diagnosis and molecular cytogenetic characterization of fetuses with central nervous system anomalies using chromosomal microarray analysis: a seven-year single-center retrospective study.
    Zhuang J; Zhang N; Chen Y; Jiang Y; Chen X; Chen W; Chen C
    Sci Rep; 2024 Jan; 14(1):2271. PubMed ID: 38280885
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Concordance of Chromosomal Microarray Analysis in Prenatal Diagnosis of Fetuses with Abnormal Ultrasonographic Soft Markers.
    Lu Y; Liu C; Ji Y
    J Coll Physicians Surg Pak; 2023 Mar; 33(3):270-274. PubMed ID: 36945155
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies.
    Sagi-Dain L; Cohen Vig L; Kahana S; Yacobson S; Tenne T; Agmon-Fishman I; Klein C; Matar R; Basel-Salmon L; Maya I
    Genet Med; 2019 Nov; 21(11):2462-2467. PubMed ID: 31123319
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Chromosome microarray analysis combined with karyotype analysis is a powerful tool for the detection in pregnant women with high-risk indicators.
    Qian G; Cai L; Yao H; Dong X
    BMC Pregnancy Childbirth; 2023 Nov; 23(1):784. PubMed ID: 37951870
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome (sSMC) inherited from her mosaic sSMC(15) mother and a literature review.
    Sun ML; Zhang HG; Liu XY; Yue FG; Jiang YT; Li SB; Liu RZ
    Taiwan J Obstet Gynecol; 2020 Nov; 59(6):963-967. PubMed ID: 33218423
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis.
    Xie X; Huang B; Su L; Cai M; Chen Y; Wu X; Xu L
    BMC Med Genomics; 2023 Nov; 16(1):298. PubMed ID: 37986075
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Validation of a Chromosomal Microarray for Prenatal Diagnosis Using a Prospective Cohort of Pregnancies with Increased Risk for Chromosome Abnormalities.
    Wright D; Carey L; Battersby S; Nguyen T; Clarke M; Nash B; Gulesserian E; Cross J; Darmanian A
    Genet Test Mol Biomarkers; 2016 Dec; 20(12):791-798. PubMed ID: 27690282
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal diagnosis of fetuses conceived by assisted reproductive technology by karyotyping and chromosomal microarray analysis.
    Guo H; Sheng R; Zhang X; Jin X; Gu W; Liu T; Dong H; Jia R
    PeerJ; 2023; 11():e14678. PubMed ID: 36684682
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Clinical value of genome-wide chromosome microarray technique in diagnosis of fetal cerebral ventriculomegaly].
    Peng YX; Qiu YW; Chang QX; Yu YH; Zhong M; Li KR
    Nan Fang Yi Ke Da Xue Xue Bao; 2018 Mar; 38(3):353-357. PubMed ID: 29643044
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Prenatal diagnosis of BACs-on-Beads assay in 1520 cases from Fujian Province, China.
    Wang Y; Zhang M; Chen L; Huang H; Xu L
    Mol Genet Genomic Med; 2020 Oct; 8(10):e1446. PubMed ID: 32767744
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations].
    Ulmer R; Pfeiffer RA; Kollert A; Beinder E
    Z Geburtshilfe Neonatol; 2000; 204(1):1-7. PubMed ID: 10721179
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Chromosomal microarray analysis and prenatal diagnosis.
    Lo JO; Shaffer BL; Feist CD; Caughey AB
    Obstet Gynecol Surv; 2014 Oct; 69(10):613-21. PubMed ID: 25336071
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Prenatal Genetic Diagnosis of Fetal Cystic Hygroma: A Retrospective Single-Center Study from China.
    Zhou Y; Lu X; Zhang Y; Ge Y; Xu Y; Wu L; Jiang Y
    Cytogenet Genome Res; 2022; 162(7):354-364. PubMed ID: 36907182
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Clinical value of genome-wide high resolution chromosomal microarray analysis in etiological study of fetuses with congenital heart defects].
    Wu X; Fu F; Li R; Pan M; Han J; Zhen L; Yang X; Zhang Y; Li F; Liao C
    Zhonghua Fu Chan Ke Za Zhi; 2014 Dec; 49(12):893-8. PubMed ID: 25608988
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Application for prenatal diagnosis using both chromosomal karyotype analysis and BACs-on-Beads assay].
    Dai W; Jiang Y; Gulinazi M; Liu X; Yu Z; Liu N; Wang L; Ma G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Jun; 35(3):357-360. PubMed ID: 29896731
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Diagnostic accuracy and value of chromosomal microarray analysis for chromosomal abnormalities in prenatal detection: A prospective clinical study.
    Huang H; Wang Y; Zhang M; Lin N; An G; He D; Chen M; Chen L; Xu L
    Medicine (Baltimore); 2021 May; 100(20):e25999. PubMed ID: 34011095
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prenatal microarray analysis as second-tier diagnostic test: single-center prospective study.
    Schmid M; Stary S; Springer S; Bettelheim D; Husslein P; Streubel B
    Ultrasound Obstet Gynecol; 2013 Mar; 41(3):267-73. PubMed ID: 23292918
    [TBL] [Abstract][Full Text] [Related]  

  • 39. BAC chromosomal microarray for prenatal detection of chromosome anomalies in fetal ultrasound anomalies: an economic evaluation.
    Hillman SC; Barton PM; Roberts TE; Maher ER; McMullan DM; Kilby MD
    Fetal Diagn Ther; 2014; 36(1):49-58. PubMed ID: 24943865
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prenatal detection of chromosomal abnormalities and copy number variants in fetuses with ventriculomegaly.
    Chang Q; Yang Y; Peng Y; Liu S; Li L; Deng X; Yang M; Lan Y
    Eur J Paediatr Neurol; 2020 Mar; 25():106-112. PubMed ID: 32014392
    [TBL] [Abstract][Full Text] [Related]  

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