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 *

165 related articles for article (PubMed ID: 35265361)

  • 1. SNP-Based Chromosomal Microarray Analysis for Detecting DNA Copy Number Variations in Fetuses with a Thickened Nuchal Fold.
    Kievskaya JK; Shilova NV; Kanivets IV; Kudryavtseva EV; Pyankov DV; Korostelev SA
    Sovrem Tekhnologii Med; 2021; 13(6):72-76. PubMed ID: 35265361
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [Analysis of copy number variation by CMA in fetus with increased nuchal translucency].
    Du L; Xie HN; Zheng J; He M
    Zhonghua Fu Chan Ke Za Zhi; 2018 Oct; 53(10):671-676. PubMed ID: 30369122
    [No Abstract]   [Full Text] [Related]  

  • 4. Application of chromosomal microarray in fetuses with increased nuchal translucency.
    Zhao XR; Gao L; Wu Y; Wang YL
    J Matern Fetal Neonatal Med; 2020 May; 33(10):1749-1754. PubMed ID: 30688128
    [No Abstract]   [Full Text] [Related]  

  • 5. Chromosomal microarray analysis versus noninvasive prenatal testing in fetuses with increased nuchal translucency.
    Wang C; Tang J; Tong K; Huang D; Tu H; Zhu J
    J Hum Genet; 2022 Sep; 67(9):533-539. PubMed ID: 35578003
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Selection of prenatal screening with nuchal translucency > 95th centile and below 99th centile: a 4-year observational study with real-world data.
    Zhang B; Zhang LX; Yi J; Wang CH; Zhao Y
    Arch Gynecol Obstet; 2024 Sep; 310(3):1779-1785. PubMed ID: 38625542
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genomic microarray in fetuses with increased nuchal translucency and normal karyotype: a systematic review and meta-analysis.
    Grande M; Jansen FA; Blumenfeld YJ; Fisher A; Odibo AO; Haak MC; Borrell A
    Ultrasound Obstet Gynecol; 2015 Dec; 46(6):650-8. PubMed ID: 25900824
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Application of chromosomal microarray analysis in 815 fetuses with increased nuchal translucency during early pregnancy].
    Yang D; Yang X; Lei T; Fu F; Li R; Li D; Liao C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Aug; 37(8):833-838. PubMed ID: 32761589
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Assessing the value of second-trimester nasal bone hypoplasia in predicting chromosomal abnormalities: a retrospective chromosomal microarray analysis of 351 fetuses.
    Pan L; Liang H; Meng Z; Wang J; Zhang R; Wu Y
    Arch Gynecol Obstet; 2023 Oct; 308(4):1263-1270. PubMed ID: 36269386
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Whole exome sequencing in fetuses with isolated increased nuchal translucency: a systematic review and meta-analysis.
    Di Girolamo R; Rizzo G; Khalil A; Alameddine S; Lisi G; Liberati M; Novelli A; D'Antonio F
    J Matern Fetal Neonatal Med; 2023 Dec; 36(1):2193285. PubMed ID: 37019452
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study.
    Egloff M; Hervé B; Quibel T; Jaillard S; Le Bouar G; Uguen K; Saliou AH; Valduga M; Perdriolle E; Coutton C; Coston AL; Coussement A; Anselem O; Missirian C; Bretelle F; Prieur F; Fanget C; Muti C; Jacquemot MC; Beneteau C; Le Vaillant C; Vekemans M; Salomon LJ; Vialard F; Malan V
    Ultrasound Obstet Gynecol; 2018 Dec; 52(6):715-721. PubMed ID: 29027723
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal Diagnostic Value of Chromosomal Microarray in Fetuses with Nuchal Translucency Greater than 2.5 mm.
    Zhang Z; Hu T; Wang J; Li Q; Wang H; Liu S
    Biomed Res Int; 2019; 2019():6504159. PubMed ID: 32908864
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Diagnostic yield of copy number variation sequencing in fetuses with increased nuchal translucency: a retrospective study.
    Yang X; Bian X; Shi X; Ding J; Tang H; Xu P; Deng D; Zeng W; Chen S; Qiao F; Feng L; Wu Y
    Arch Gynecol Obstet; 2024 Jan; 309(1):139-144. PubMed ID: 36602560
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Should prenatal chromosomal microarray analysis be offered for isolated fetal growth restriction? A French multicenter study.
    Monier I; Receveur A; Houfflin-Debarge V; Goua V; Castaigne V; Jouannic JM; Mousty E; Saliou AH; Bouchghoul H; Rousseau T; Valat AS; Groussolles M; Fuchs F; Benoist G; Degre S; Massardier J; Tsatsaris V; Kleinfinger P; Zeitlin J; Benachi A;
    Am J Obstet Gynecol; 2021 Dec; 225(6):676.e1-676.e15. PubMed ID: 34058167
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings.
    Hui AS; Chau MHK; Chan YM; Cao Y; Kwan AH; Zhu X; Kwok YK; Chen Z; Lao TT; Choy KW; Leung TY
    Acta Obstet Gynecol Scand; 2021 Feb; 100(2):235-243. PubMed ID: 32981064
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of copy number variation by sequencing in fetuses with nuchal translucency thickening.
    Lan L; Wu H; She L; Zhang B; He Y; Luo D; Wang H; Zheng Z
    J Clin Lab Anal; 2020 Aug; 34(8):e23347. PubMed ID: 32342531
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Application of chromosome microarray analysis for fetuses with increased nuchal translucency and a normal karyotype].
    Yang X; Fu F; Li R; Zhang Y; Wan J; Yang X; Han J; Pan M; Zhen L; Liao C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):370-4. PubMed ID: 26037353
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [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]  

  • 19. Clinical utility of array comparative genomic hybridisation in prenatal setting.
    Lovrecic L; Remec ZI; Volk M; Rudolf G; Writzl K; Peterlin B
    BMC Med Genet; 2016 Nov; 17(1):81. PubMed ID: 27846804
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.