BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 30519285)

  • 1. Chromosomal abnormalities and copy number variations in fetal ventricular septal defects.
    Cai M; Huang H; Su L; Lin N; Wu X; Xie X; An G; Li Y; Lin Y; Xu L; Cao H
    Mol Cytogenet; 2018; 11():58. PubMed ID: 30519285
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal diagnosis of submicroscopic chromosomal aberrations in fetuses with ventricular septal defects by chromosomal microarray-based analysis.
    Du L; Xie HN; Huang LH; Xie YJ; Wu LH
    Prenat Diagn; 2016 Dec; 36(13):1178-1184. PubMed ID: 27794163
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical application of SNP array analysis in fetuses with ventricular septal defects and normal karyotypes.
    Fu F; Deng Q; Lei TY; Li R; Jing XY; Yang X; Liao C
    Arch Gynecol Obstet; 2017 Nov; 296(5):929-940. PubMed ID: 28905115
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Should prenatal chromosomal microarray analysis be offered for isolated ventricular septal defect? A single-center retrospective study from China.
    Cheng K; Zhou H; Fu F; Lei T; Li F; Huang R; Wang Y; Yang X; Li R; Li D; Liao C
    Front Cardiovasc Med; 2022; 9():988438. PubMed ID: 36158810
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Application of chromosomal microarray analysis for fetuses with ventricular septal defects].
    Deng Q; Fu F; Li R; Jing X; Lei T; Yang X; Pan M; Zhen L; Han J; Liao C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct; 34(5):699-704. PubMed ID: 28981937
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Correlation between types of ventricular septal defect and chromosomal abnormalities in low-risk non-invasive prenatal testing.
    Zhao X; Shen Y; Kong D; Li W; Yao L; Li S; Chang Y
    Arch Gynecol Obstet; 2024 Jun; ():. PubMed ID: 38922412
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chromosomal Microarray Analysis for the Prenatal Diagnosis in Fetuses with Nasal Bone Hypoplasia: A Retrospective Cohort Study.
    Huang H; Cai M; Ma W; Lin N; Xu L
    Risk Manag Healthc Policy; 2021; 14():1533-1540. PubMed ID: 33889037
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal genetic diagnosis associated with fetal ventricular septal defect: an assessment based on chromosomal microarray analysis and exome sequencing.
    Wang Y; Li R; Fu F; Huang R; Li D; Liao C
    Front Genet; 2023; 14():1260995. PubMed ID: 38075692
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Application of chromosome microarray analysis in prenatal diagnosis.
    Xia M; Yang X; Fu J; Teng Z; Lv Y; Yu L
    BMC Pregnancy Childbirth; 2020 Nov; 20(1):696. PubMed ID: 33198662
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fetal congenital heart disease: Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcome.
    Cai M; Huang H; Su L; Lin N; Wu X; Xie X; An G; Li Y; Lin Y; Xu L
    Medicine (Baltimore); 2018 Dec; 97(50):e13617. PubMed ID: 30558042
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical application of chromosomal microarray analysis for the prenatal diagnosis of chromosomal abnormalities and copy number variations in fetuses with congenital heart disease.
    Xia Y; Yang Y; Huang S; Wu Y; Li P; Zhuang J
    Prenat Diagn; 2018 May; 38(6):406-413. PubMed ID: 29573438
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Correlation between mild fetal ventriculomegaly, chromosomal abnormalities, and copy number variations.
    Huang RN; Chen JY; Pan H; Liu QQ
    J Matern Fetal Neonatal Med; 2022 Dec; 35(24):4788-4796. PubMed ID: 33371747
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of chromosomal aberrations in fetuses with conotruncal heart defects by genome-wide high-resolution SNP array.
    Lin M; Zheng J; Peng R; Du L; Zheng Q; Lei T; Xie H
    J Matern Fetal Neonatal Med; 2020 Apr; 33(7):1211-1217. PubMed ID: 30149741
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Prenatal diagnosis of submicroscopic chromosomal aberrations in fetuses with congenital cystic adenomatoid malformation by chromosomal microarray analysis.
    Deng Q; Huang L; Liu J; Fang F; Liu Z; Zhang Y; Li F; Liao C
    J Matern Fetal Neonatal Med; 2021 Aug; 34(16):2623-2629. PubMed ID: 31581877
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Effectiveness of Chromosomal Microarray Analysis for Prenatal Diagnosis of Fetal Echogenic Intracardiac Focus: A Single-Center Experience.
    Huang H; Cai M; Liu L; Xu L; Lin N
    Int J Gen Med; 2021; 14():1991-1997. PubMed ID: 34045891
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.