These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

178 related articles for article (PubMed ID: 34365628)

  • 1. [Association of fetal cardiac structural abnormalities and chromosomal aneuploidies and copy number variations].
    Hou R; Kong F; Zhao S; Guo H; Wang S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Aug; 38(8):795-797. PubMed ID: 34365628
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. [The value of non-invasive prenatal testing for the identification of numerical and structural chromosomal abnormalities and copy number variations in the fetuses].
    Hou S; Zhang H; Li C; Chen D; Yan H; Yang M; Liu Y; Lei D
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Oct; 40(10):1197-1203. PubMed ID: 37730217
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chromosomal aneuploidies and copy number variations in posterior fossa abnormalities diagnosed by prenatal ultrasonography.
    Lei T; Feng JL; Xie YJ; Xie HN; Zheng J; Lin MF
    Prenat Diagn; 2017 Nov; 37(11):1160-1168. PubMed ID: 28940600
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Influence of maternal chromosomal abnormalities on non-invasive prenatal testing for fetal sex chromosome aneuploidies].
    Yuan P; Zhang B; Liu J; Wang H; Lu B; Zhou Q; Yu B; Cai Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jun; 37(6):617-620. PubMed ID: 32472536
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. [Application of high-throughput sequencing technology for the detection of fetal copy number variations].
    Jiang N; Zhang Y; Song L; Yu D
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jul; 37(7):779-784. PubMed ID: 32619264
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Defining the scope of extended NIPS in Western China: evidence from a large cohort of fetuses with normal ultrasound scans.
    Chen L; Wang L; Zeng Y; Yin D; Tang F; Xie D; Zhu H; Liu H; Wang J
    BMC Pregnancy Childbirth; 2023 Aug; 23(1):593. PubMed ID: 37598172
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. [Prenatal genetic diagnosis for fetuses with anomalies revealed by fetal echocardiography].
    Jiang Q; Yuan L; Yu H; Yang X; Cao D
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Dec; 39(12):1324-1328. PubMed ID: 36453952
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Copy number variations in ultrasonically abnormal late pregnancy fetuses with normal karyotypes.
    Cai M; Lin N; Su L; Wu X; Xie X; Li Y; Lin Y; Xu L; Huang H
    Sci Rep; 2020 Sep; 10(1):15094. PubMed ID: 32934329
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection of fetal copy number variants by non-invasive prenatal testing for common aneuploidies.
    Li R; Wan J; Zhang Y; Fu F; Ou Y; Jing X; Li J; Li D; Liao C
    Ultrasound Obstet Gynecol; 2016 Jan; 47(1):53-7. PubMed ID: 26033469
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Application of chromosomal microarray analysis in prenatal diagnosis of fetuses with increased nuchal translucency].
    Ni M; Li J; Zhu X; Zhu Y; Gu L; Wu X; Yang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Oct; 36(10):970-974. PubMed ID: 31598938
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Analysis of tissue from pregnancy loss and aborted fetus with ultrasound anomaly using subtelomeric MLPA and chromosomal array analysis.
    Lou J; Sun M; Zhao Y; Fu Y; Yuan H; Dai Y; Liang F; He Y; Liu Y
    J Matern Fetal Neonatal Med; 2022 Aug; 35(16):3064-3069. PubMed ID: 32811234
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Application of chromosomal microarray analysis in prenatal diagnosis for fetal abnormalities detected by ultrasonography].
    Hu T; Wang J; Zhang Z; Zhu H; Liu H; Zhang X; Zhang H; Du Z; Li L; Wang H; Liu S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Jun; 34(3):317-320. PubMed ID: 28604946
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Whole genome sequencing vs chromosomal microarray analysis in prenatal diagnosis.
    Hu P; Zhang Q; Cheng Q; Luo C; Zhang C; Zhou R; Meng L; Huang M; Wang Y; Wang Y; Qiao F; Xu Z
    Am J Obstet Gynecol; 2023 Sep; 229(3):302.e1-302.e18. PubMed ID: 36907537
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.