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 *

247 related articles for article (PubMed ID: 34374610)

  • 1. 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]  

  • 2. 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]  

  • 3. Ultrasonographic characteristics, genetic features, and maternal and fetal outcomes in fetuses with omphalocele in China: a single tertiary center study.
    Que Y; Cai M; Yang F; Ji Q; Zhang S; Huang W; Gao Y; Zhou B; Huang H; Cao H; Lin N
    BMC Pregnancy Childbirth; 2023 Sep; 23(1):679. PubMed ID: 37726736
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Whole Genome Sequencing in the Evaluation of Fetal Structural Anomalies: A Parallel Test with Chromosomal Microarray Plus Whole Exome Sequencing.
    Zhou J; Yang Z; Sun J; Liu L; Zhou X; Liu F; Xing Y; Cui S; Xiong S; Liu X; Yang Y; Wei X; Zou G; Wang Z; Wei X; Wang Y; Zhang Y; Yan S; Wu F; Zeng F; Wang J; Duan T; Peng Z; Sun L
    Genes (Basel); 2021 Mar; 12(3):. PubMed ID: 33800913
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [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]  

  • 7. 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]  

  • 8. Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.
    Hillman SC; McMullan DJ; Hall G; Togneri FS; James N; Maher EJ; Meller CH; Williams D; Wapner RJ; Maher ER; Kilby MD
    Ultrasound Obstet Gynecol; 2013 Jun; 41(6):610-20. PubMed ID: 23512800
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chromosomal abnormalities detected by karyotyping and microarray analysis in twins with structural anomalies.
    Li L; He Z; Huang X; Lin S; Wu J; Huang L; Wan Y; Fang Q
    Ultrasound Obstet Gynecol; 2020 Apr; 55(4):502-509. PubMed ID: 30977228
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Prenatal genetic testing in 19 fetuses with corpus callosum abnormality.
    She Q; Tang E; Peng C; Wang L; Wang D; Tan W
    J Clin Lab Anal; 2021 Nov; 35(11):e23971. PubMed ID: 34569664
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic diagnosis of common fetal renal abnormalities detected on prenatal ultrasound.
    Liu L; Li J; Li Y; Li H; Yang B; Fan H; Wang J; Gu Y; Yu H; Bai M; Yu T; Cui S; Cheng G; Ren C
    Prenat Diagn; 2022 Jun; 42(7):894-900. PubMed ID: 35478332
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Prenatal chromosomal microarray analysis and karyotyping in fetuses with isolated choroid plexus cyst: A retrospective case-control study.
    Wang L; Liang P; Pan P; Su J; Qin J; Chen Z; Huang D; Sun W; Song P; Wei H
    Eur J Obstet Gynecol Reprod Biol; 2024 Jun; 297():91-95. PubMed ID: 38603985
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The clinical use of chromosomal microarray analysis in detection of fetal chromosomal rearrangements: a study from China Mainland.
    Wu Y; Wang Y; Tao J; Han X; Zhao X; Liu C; Gao L; Cheng W
    Eur J Obstet Gynecol Reprod Biol; 2017 May; 212():44-50. PubMed ID: 28340467
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical utility of chromosomal microarray analysis and whole exome sequencing in foetuses with oligohydramnios.
    Shi X; Ding H; Li C; Liu L; Yu L; Zhu J; Wu J
    Ann Med; 2023 Dec; 55(1):2215539. PubMed ID: 37243546
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes.
    Qi Q; Jiang Y; Zhou X; Meng H; Hao N; Chang J; Bai J; Wang C; Wang M; Guo J; Ouyang Y; Xu Z; Xiao M; Zhang VW; Liu J
    Genes (Basel); 2020 Nov; 11(12):. PubMed ID: 33255631
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Application of chromosomal microarray analysis in prenatal diagnosis of fetal growth restriction.
    Zhu H; Lin S; Huang L; He Z; Huang X; Zhou Y; Fang Q; Luo Y
    Prenat Diagn; 2016 Jul; 36(7):686-92. PubMed ID: 27221052
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing.
    Wang J; Chen L; Zhou C; Wang L; Xie H; Xiao Y; Zhu H; Hu T; Zhang Z; Zhu Q; Liu Z; Liu S; Wang H; Xu M; Ren Z; Yu F; Cram DS; Liu H
    Am J Obstet Gynecol; 2018 Sep; 219(3):287.e1-287.e18. PubMed ID: 29852155
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.