BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

169 related articles for article (PubMed ID: 27977861)

  • 1. A copy number variation genotyping method for aneuploidy detection in spontaneous abortion specimens.
    Chen S; Liu D; Zhang J; Li S; Zhang L; Fan J; Luo Y; Qian Y; Huang H; Liu C; Zhu H; Jiang Z; Xu C
    Prenat Diagn; 2017 Feb; 37(2):176-183. PubMed ID: 27977861
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Detection of chromosomal abnormalities in spontaneous miscarriage by low‑coverage next‑generation sequencing.
    Li FX; Xie MJ; Qu SF; He D; Wu L; Liang ZK; Wu YS; Yang F; Yang XX
    Mol Med Rep; 2020 Aug; 22(2):1269-1276. PubMed ID: 32626971
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of Chromosomal Abnormalities in Early Pregnancy Loss Using a High-Throughput Ligation-Dependent Probe Amplification-Based Assay.
    Wang Y; Zhou R; Jiang L; Meng L; Tan J; Qiao F; Wang Y; Zhang C; Cheng Q; Jiang Z; Hu P; Xu Z
    J Mol Diagn; 2021 Jan; 23(1):38-45. PubMed ID: 33069876
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Application of next generation sequencing for the detection of chromosomal aneuploidies and copy number variations in abortus tissues].
    Chen J; Hu L; Yang J; Liu P
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Aug; 35(4):591-594. PubMed ID: 30098263
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Traditional karyotyping vs copy number variation sequencing for detection of chromosomal abnormalities associated with spontaneous miscarriage.
    Liu S; Song L; Cram DS; Xiong L; Wang K; Wu R; Liu J; Deng K; Jia B; Zhong M; Yang F
    Ultrasound Obstet Gynecol; 2015 Oct; 46(4):472-7. PubMed ID: 25767059
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Application of array-based comparative genomic hybridization technique in genetic analysis of patients with spontaneous abortion].
    Chu Y; Wu D; Hou QF; Huo XD; Gao Y; Wang T; Wang HD; Yang YL; Liao SX
    Zhonghua Fu Chan Ke Za Zhi; 2016 Aug; 51(8):592-6. PubMed ID: 27561938
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prevalence of chromosomal abnormalities identified by copy number variation sequencing in high-risk pregnancies, spontaneous abortions, and suspected genetic disorders.
    Zhang R; Chen X; Wang D; Chen X; Wang C; Zhang Y; Xu M; Yu J
    J Int Med Res; 2019 Mar; 47(3):1169-1178. PubMed ID: 30732499
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Analysis of genetic etiology and related factors in 1 065 women with spontaneous abortions].
    Ding H; Duan H; Zhu X; Liu W; Gu L; Li H; Jiang Z; Li J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Apr; 40(4):446-451. PubMed ID: 36972940
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Detection for chromosomal aberrations in 43 fetuses with spontaneous abortion and stillbirth by array-based comparative genomic hybridization].
    Li Y; Gong Y; Liu H; Song Y; He W; Wei J; Sun X; Chen X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):348-52. PubMed ID: 26037348
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Diagnostic utility of microarray testing in pregnancy loss.
    Rosenfeld JA; Tucker ME; Escobar LF; Neill NJ; Torchia BS; McDaniel LD; Schultz RA; Chong K; Chitayat D
    Ultrasound Obstet Gynecol; 2015 Oct; 46(4):478-86. PubMed ID: 25846569
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Why do euploid embryos miscarry? A case-control study comparing the rate of aneuploidy within presumed euploid embryos that resulted in miscarriage or live birth using next-generation sequencing.
    Maxwell SM; Colls P; Hodes-Wertz B; McCulloh DH; McCaffrey C; Wells D; Munné S; Grifo JA
    Fertil Steril; 2016 Nov; 106(6):1414-1419.e5. PubMed ID: 27692437
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cytogenetic Analysis of the Products of Conception After Spontaneous Abortion in the First Trimester.
    Zhang X; Fan J; Chen Y; Wang J; Song Z; Zhao J; Li Z; Wu X; Hu Y
    Cytogenet Genome Res; 2021; 161(3-4):120-131. PubMed ID: 33975305
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Low aneuploidy rate in early pregnancy loss abortuses from patients with polycystic ovary syndrome.
    Wang Q; Luo L; Lei Q; Lin MM; Huang X; Chen MH; Zeng YH; Zhou CQ
    Reprod Biomed Online; 2016 Jul; 33(1):85-92. PubMed ID: 27157933
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant women.
    Kølvraa S; Singh R; Normand EA; Qdaisat S; van den Veyver IB; Jackson L; Hatt L; Schelde P; Uldbjerg N; Vestergaard EM; Zhao L; Chen R; Shaw CA; Breman AM; Beaudet AL
    Prenat Diagn; 2016 Dec; 36(12):1127-1134. PubMed ID: 27761919
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Semiconductor Sequencing Analysis of Chromosomal Copy Number Variations in Spontaneous Miscarriage.
    Wang MZ; Lin FQ; Li M; He D; Yu QH; Yang XX; Wu YS
    Med Sci Monit; 2017 Nov; 23():5550-5557. PubMed ID: 29162795
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sequential application of copy number variation sequencing and quantitative fluorescence polymerase chain reaction in genetic analysis of miscarriage and stillbirth.
    Chen Q; Zhang H; Li X; Li J; Chen H; Liu L; Zhou S; Xu Z
    Mol Genet Genomic Med; 2023 Aug; 11(8):e2187. PubMed ID: 37073418
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Noninvasive Prenatal Testing of Rare Autosomal Aneuploidies by Semiconductor Sequencing.
    Xie MJ; Liang ZK; He D; Xu WW; Wu YS; Yang XX; Li M
    DNA Cell Biol; 2018 Mar; 37(3):174-181. PubMed ID: 29381401
    [TBL] [Abstract][Full Text] [Related]  

  • 18. First-trimester spontaneous pregnancy loss - molecular analysis using multiplex ligation-dependent probe amplification.
    Zimowski JG; Massalska D; Pawelec M; Bijok J; Michałowska A; Roszkowski T
    Clin Genet; 2016 May; 89(5):620-4. PubMed ID: 26748861
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Utility and limitations of multiplex ligation-dependent probe amplification technique in the detection of cytogenetic abnormalities in products of conception.
    Saxena D; Agarwal M; Gupta D; Agrawal S; Das V; Phadke SR
    J Postgrad Med; 2016; 62(4):239-241. PubMed ID: 27763481
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Chromosomal abnormalities in spontaneous miscarriage specimens detected by combinatorial probe anchor synthesis-based high-throughput low coverage whole genome sequencing].
    Wang XH; Bai RF; Zhou Y; Dong H; Ji YP; Hou DX; Wu RGML; Yang XL; Ji XP
    Zhonghua Fu Chan Ke Za Zhi; 2019 Dec; 54(12):808-814. PubMed ID: 31874470
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.