BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

300 related articles for article (PubMed ID: 34983622)

  • 1. Estimating the frequency of causal genetic variants in foetuses with congenital heart defects: a Chinese cohort study.
    Lu F; Xue P; Zhang B; Wang J; Yu B; Liu J
    Orphanet J Rare Dis; 2022 Jan; 17(1):2. PubMed ID: 34983622
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Comprehensive evaluation of genetic variants using chromosomal microarray analysis and exome sequencing in fetuses with congenital heart defect.
    Qiao F; Wang Y; Zhang C; Zhou R; Wu Y; Wang C; Meng L; Mao P; Cheng Q; Luo C; Hu P; Xu Z
    Ultrasound Obstet Gynecol; 2021 Sep; 58(3):377-387. PubMed ID: 33142350
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencing.
    Zhu X; Li J; Ru T; Wang Y; Xu Y; Yang Y; Wu X; Cram DS; Hu Y
    Prenat Diagn; 2016 Apr; 36(4):321-7. PubMed ID: 26833920
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Congenital heart defects and copy number variants associated with neurodevelopmental impairment.
    Findley TO; Crain AK; Mahajan S; Deniwar A; Davis J; Solis Zavala AS; Corno AF; Rodriguez-Buritica D
    Am J Med Genet A; 2022 Jan; 188(1):13-23. PubMed ID: 34472185
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Yield rate of chromosomal microarray analysis in fetuses with congenital heart defects.
    Turan S; Asoglu MR; Gabbay-Benziv R; Doyle L; Harman C; Turan OM
    Eur J Obstet Gynecol Reprod Biol; 2018 Feb; 221():172-176. PubMed ID: 29306563
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Association of prenatal renal ultrasound abnormalities with pathogenic copy number variants in a large Chinese cohort.
    Su J; Qin Z; Fu H; Luo J; Huang Y; Huang P; Zhang S; Liu T; Lu W; Li W; Jiang T; Wei S; Yang S; Shen Y
    Ultrasound Obstet Gynecol; 2022 Feb; 59(2):226-233. PubMed ID: 34090309
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The yield of SNP microarray analysis for fetal ultrasound cardiac abnormalities.
    Ye F; Xu X; Wang Y; Chen L; Shan Q; Wang Q; Jin F
    BMC Pregnancy Childbirth; 2024 Apr; 24(1):244. PubMed ID: 38580914
    [TBL] [Abstract][Full Text] [Related]  

  • 8. MLPA analysis of 32 foetuses with a congenital heart defect and 1 foetus with renal defects - pilot study. The significant frequency rate of presented pathological CNV.
    Stefekova A; Capkova P; Capkova Z; Curtisova V; Srovnal J; Mracka E; Klaskova E; Prochazka M
    Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub; 2022 May; 166(2):187-194. PubMed ID: 33824538
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic Testing and Pregnancy Outcome Analysis of 362 Fetuses with Congenital Heart Disease Identified by Prenatal Ultrasound.
    Luo S; Meng D; Li Q; Hu X; Chen Y; He C; Xie B; She S; Li Y; Fu C
    Arq Bras Cardiol; 2018 Oct; 111(4):571-577. PubMed ID: 30133550
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. Chromosomal abnormalities in fetuses with congenital heart disease: a meta-analysis.
    Wang H; Lin X; Lyu G; He S; Dong B; Yang Y
    Arch Gynecol Obstet; 2023 Sep; 308(3):797-811. PubMed ID: 36609702
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chromosomal microarray analysis in fetuses with an isolated congenital heart defect: A retrospective, nationwide, multicenter study in France.
    Hureaux M; Guterman S; Hervé B; Till M; Jaillard S; Redon S; Valduga M; Coutton C; Missirian C; Prieur F; Simon-Bouy B; Beneteau C; Kuentz P; Rooryck C; Gruchy N; Marle N; Plutino M; Tosca L; Dupont C; Puechberty J; Schluth-Bolard C; Salomon L; Sanlaville D; Malan V; Vialard F
    Prenat Diagn; 2019 May; 39(6):464-470. PubMed ID: 30896039
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic aetiology distribution of 398 foetuses with congenital heart disease in the prenatal setting.
    Yi T; Hao X; Sun H; Zhang Y; Han J; Gu X; Sun L; Liu X; Zhao Y; Guo Y; Zhou X; He Y
    ESC Heart Fail; 2023 Apr; 10(2):917-930. PubMed ID: 36478645
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection of submicroscopic chromosomal aberrations by array-based comparative genomic hybridization in fetuses with congenital heart disease.
    Yan Y; Wu Q; Zhang L; Wang X; Dan S; Deng D; Sun L; Yao L; Ma Y; Wang L
    Ultrasound Obstet Gynecol; 2014 Apr; 43(4):404-12. PubMed ID: 24323407
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield.
    Geng J; Picker J; Zheng Z; Zhang X; Wang J; Hisama F; Brown DW; Mullen MP; Harris D; Stoler J; Seman A; Miller DT; Fu Q; Roberts AE; Shen Y
    BMC Genomics; 2014 Dec; 15(1):1127. PubMed ID: 25516202
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis for fetuses with isolated and non-isolated congenital heart defects using chromosomal microarray and exome sequencing.
    Xing Y; Zhang Y; Chen J; Wu F; Yuan M; Zou G; Yang Y; Zhou F; Zhou J; Sun L
    Prenat Diagn; 2022 Jun; 42(7):873-880. PubMed ID: 35584285
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Contribution of genetic variants to congenital heart defects in both singleton and twin fetuses: a Chinese cohort study.
    Lin S; Shi S; Lu J; He Z; Li D; Huang L; Huang X; Zhou Y; Luo Y
    Mol Cytogenet; 2024 Jan; 17(1):2. PubMed ID: 38178226
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Copy number variant analysis for syndromic congenital heart disease in the Chinese population.
    Li P; Chen W; Li M; Zhao Z; Feng Z; Gao H; Suo M; Xu Z; Tian G; Wu F; Wei S; Huang G
    Hum Genomics; 2022 Oct; 16(1):51. PubMed ID: 36316717
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal genetic diagnosis of omphalocele by karyotyping, chromosomal microarray analysis and exome sequencing.
    Shi X; Tang H; Lu J; Yang X; Ding H; Wu J
    Ann Med; 2021 Dec; 53(1):1285-1291. PubMed ID: 34374610
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.