BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

700 related articles for article (PubMed ID: 24323407)

  • 21. 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]  

  • 22. 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]  

  • 23. [Combined G-banded karyotyping and multiplex ligation-dependent probe amplification for the detection of chromosomal abnormalities in fetuses with congenital heart defects].
    Liu Y; Xie J; Geng Q; Xu Z; Wu W; Luo F; Li S; Wang Q; Chen W; Tan H; Zhang H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):1-5. PubMed ID: 28186583
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Prenatal chromosomal microarray analysis in fetuses with congenital heart disease: a prospective cohort study.
    Wang Y; Cao L; Liang D; Meng L; Wu Y; Qiao F; Ji X; Luo C; Zhang J; Xu T; Yu B; Wang L; Wang T; Pan Q; Ma D; Hu P; Xu Z
    Am J Obstet Gynecol; 2018 Feb; 218(2):244.e1-244.e17. PubMed ID: 29128521
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects.
    Hussein IR; Bader RS; Chaudhary AG; Bassiouni R; Alquaiti M; Ashgan F; Schulten HJ; Al Qahtani MH
    Pediatr Cardiol; 2018 Jun; 39(5):924-940. PubMed ID: 29541814
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cardiovascular Anomalies among 1005 Fetuses Referred to Invasive Prenatal Testing-A Comprehensive Cohort Study of Associated Chromosomal Aberrations.
    Wójtowicz A; Madetko-Talowska A; Wójtowicz W; Szewczyk K; Huras H; Bik-Multanowski M
    Int J Environ Res Public Health; 2022 Aug; 19(16):. PubMed ID: 36011653
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 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]  

  • 30. Detection of copy number variants using chromosomal microarray analysis for the prenatal diagnosis of congenital heart defects with normal karyotype.
    Song T; Wan S; Li Y; Xu Y; Dang Y; Zheng Y; Li C; Zheng J; Chen B; Zhang J
    J Clin Lab Anal; 2019 Jan; 33(1):e22630. PubMed ID: 30047171
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.
    D'Amours G; Kibar Z; Mathonnet G; Fetni R; Tihy F; Désilets V; Nizard S; Michaud JL; Lemyre E
    Clin Genet; 2012 Feb; 81(2):128-41. PubMed ID: 21496010
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The frequency of CNVs in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancy.
    Rudolf G; Lovrečić L; Tul N; Teran N; Peterlin B
    Mol Genet Genomic Med; 2019 Jun; 7(6):e658. PubMed ID: 31004418
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [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]  

  • 34. 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]  

  • 35. 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]  

  • 36. [Application of array comparative genomic hybridization analysis for fetuses with growth anomalies].
    Wang L; Wang X; Cai N; He B; Wu Q; Li W; Zhang L; Ma X; Qiang R
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct; 34(5):691-694. PubMed ID: 28981935
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Challenges of interpreting copy number variation in syndromic and non-syndromic congenital heart defects.
    Breckpot J; Thienpont B; Arens Y; Tranchevent LC; Vermeesch JR; Moreau Y; Gewillig M; Devriendt K
    Cytogenet Genome Res; 2011; 135(3-4):251-9. PubMed ID: 21921585
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype.
    Wu X; Li Y; Su L; Xie X; Cai M; Lin N; Huang H; Lin Y; Xu L
    Mol Diagn Ther; 2020 Oct; 24(5):611-619. PubMed ID: 32651932
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prenatal detection of chromosomal abnormalities and copy number variants in fetuses with congenital gastrointestinal obstruction.
    Meng X; Jiang L
    BMC Pregnancy Childbirth; 2022 Jan; 22(1):50. PubMed ID: 35045821
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [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]  

    [Previous]   [Next]    [New Search]
    of 35.