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 *

251 related articles for article (PubMed ID: 34367232)

  • 1. The Added Value of Whole-Exome Sequencing for Anomalous Fetuses With Detailed Prenatal Ultrasound and Postnatal Phenotype.
    He M; Du L; Xie H; Zhang L; Gu Y; Lei T; Zheng J; Chen D
    Front Genet; 2021; 12():627204. PubMed ID: 34367232
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
    Petrovski S; Aggarwal V; Giordano JL; Stosic M; Wou K; Bier L; Spiegel E; Brennan K; Stong N; Jobanputra V; Ren Z; Zhu X; Mebane C; Nahum O; Wang Q; Kamalakaran S; Malone C; Anyane-Yeboa K; Miller R; Levy B; Goldstein DB; Wapner RJ
    Lancet; 2019 Feb; 393(10173):758-767. PubMed ID: 30712878
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
    Lord J; McMullan DJ; Eberhardt RY; Rinck G; Hamilton SJ; Quinlan-Jones E; Prigmore E; Keelagher R; Best SK; Carey GK; Mellis R; Robart S; Berry IR; Chandler KE; Cilliers D; Cresswell L; Edwards SL; Gardiner C; Henderson A; Holden ST; Homfray T; Lester T; Lewis RA; Newbury-Ecob R; Prescott K; Quarrell OW; Ramsden SC; Roberts E; Tapon D; Tooley MJ; Vasudevan PC; Weber AP; Wellesley DG; Westwood P; White H; Parker M; Williams D; Jenkins L; Scott RH; Kilby MD; Chitty LS; Hurles ME; Maher ER;
    Lancet; 2019 Feb; 393(10173):747-757. PubMed ID: 30712880
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Whole exome sequencing as a diagnostic adjunct to clinical testing in fetuses with structural abnormalities.
    Fu F; Li R; Li Y; Nie ZQ; Lei T; Wang D; Yang X; Han J; Pan M; Zhen L; Ou Y; Li J; Li FT; Jing X; Li D; Liao C
    Ultrasound Obstet Gynecol; 2018 Apr; 51(4):493-502. PubMed ID: 28976722
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Prenatal genetic diagnosis of the fetuses with isolated corpus callosum abnormality].
    She Q; Zhen L; Fu F; Lei TY; Li LS; Li R; Wang D; Zhang YL; Jing XY; Yi CX; Zhong HZ; Tan WH; Li FG; Liao C
    Zhonghua Fu Chan Ke Za Zhi; 2022 Sep; 57(9):671-677. PubMed ID: 36177578
    [No Abstract]   [Full Text] [Related]  

  • 6. Prenatal trio-based whole exome sequencing in fetuses with abnormalities of the skeletal system.
    Yang Y; Wang M; Wang H
    Mol Genet Genomics; 2022 Jul; 297(4):1017-1026. PubMed ID: 35583673
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal genetic diagnosis of fetuses with dextrocardia using whole exome sequencing in a tertiary center.
    Xue H; Yu A; Chen L; Guo Q; Zhang L; Lin N; Chen X; Xu L; Huang H
    Sci Rep; 2024 Jul; 14(1):16266. PubMed ID: 39009665
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Importance of complete phenotyping in prenatal whole exome sequencing.
    Aarabi M; Sniezek O; Jiang H; Saller DN; Bellissimo D; Yatsenko SA; Rajkovic A
    Hum Genet; 2018 Feb; 137(2):175-181. PubMed ID: 29392406
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Incremental yield of whole-genome sequencing over chromosomal microarray analysis and exome sequencing for congenital anomalies in prenatal period and infancy: systematic review and meta-analysis.
    Shreeve N; Sproule C; Choy KW; Dong Z; Gajewska-Knapik K; Kilby MD; Mone F
    Ultrasound Obstet Gynecol; 2024 Jan; 63(1):15-23. PubMed ID: 37725747
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Whole-exome sequencing increases the diagnostic rate for prenatal fetal structural anomalies.
    Lei L; Zhou L; Xiong JJ
    Eur J Med Genet; 2021 Sep; 64(9):104288. PubMed ID: 34246755
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Analysis of families with fetal congenital abnormalities but negative prenatal diagnosis by whole exome sequencing].
    Fu F; Li LS; Du K; Li R; Yu QX; Wang D; Lei TY; Deng Q; Nie ZQ; Zhang WW; Yang X; Han J; Zhen L; Pan M; Zhang LN; Li FC; Zhang YL; Jing XY; Li DZ; Liao C
    Zhonghua Fu Chan Ke Za Zhi; 2021 Jul; 56(7):458-466. PubMed ID: 34304437
    [No Abstract]   [Full Text] [Related]  

  • 12. Utility of trio-based prenatal exome sequencing incorporating splice-site and mitochondrial genome assessment in pregnancies with fetal ultrasound anomalies: prospective cohort study.
    Zhu X; Gao Z; Wang Y; Huang W; Li Q; Jiao Z; Liu N; Kong X
    Ultrasound Obstet Gynecol; 2022 Dec; 60(6):780-792. PubMed ID: 35726512
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Diagnostic Yield of Exome Sequencing in Fetuses with Sonographic Features of Skeletal Dysplasias but Normal Karyotype or Chromosomal Microarray Analysis: A Systematic Review.
    Tse KY; Surya IU; Irwinda R; Leung KY; Ting YH; Cao Y; Choy KW
    Genes (Basel); 2023 May; 14(6):. PubMed ID: 37372383
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis of fetuses with ultrasound anomalies by whole-exome sequencing in Luoyang city, China.
    Wang Y; Yin F; Chai Y; Jin J; Zhang P; Tan Q; Chen Z
    Front Genet; 2023; 14():1301439. PubMed ID: 38318287
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. Prenatal whole-exome sequencing in fetuses with increased nuchal translucency.
    Cao C; Liu F; Yang Y; Zhang Q; Huang J; Liu X
    Mol Genet Genomic Med; 2023 Nov; 11(11):e2246. PubMed ID: 37766479
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal whole-exome sequencing for fetal structural anomalies: a retrospective analysis of 145 Chinese cases.
    Qin Y; Yao Y; Liu N; Wang B; Liu L; Li H; Gao T; Xu R; Wang X; Zhang F; Song J
    BMC Med Genomics; 2023 Oct; 16(1):262. PubMed ID: 37880672
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis and outcomes in fetuses with duplex kidney.
    Ma C; Huang R; Fu F; Zhou H; Wang Y; Yan S; Guo F; Chen H; Li L; Jing X; Li F; Han J; Li D; Li R; Liao C
    Int J Gynaecol Obstet; 2024 Jul; 166(1):353-359. PubMed ID: 38189110
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Whole-exome sequencing in deceased fetuses with ultrasound anomalies: a retrospective analysis.
    Huang W; Zhu X; Sun G; Gao Z; Kong X
    BMC Med Genomics; 2023 Feb; 16(1):25. PubMed ID: 36797717
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Optimal prenatal genetic diagnostic approach for posterior fossa malformation: karyotyping, copy number variant testing, or whole-exome sequencing?
    Juan Z; Cuixia G; Yuanjie C; Yan L; Ling Y; Tiejuan Z; Li W; Jijing H; Guohui Z; Yousheng Y; Qingqing W; Lijuan S
    Eur J Med Res; 2024 Jul; 29(1):397. PubMed ID: 39085968
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.