BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

209 related articles for article (PubMed ID: 23780398)

  • 1. First-trimester euploid miscarriages analysed by array-CGH.
    Viaggi CD; Cavani S; Malacarne M; Floriddia F; Zerega G; Baldo C; Mogni M; Castagnetta M; Piombo G; Coviello DA; Camandona F; Lijoi D; Insegno W; Traversa M; Pierluigi M
    J Appl Genet; 2013 Aug; 54(3):353-9. PubMed ID: 23780398
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages.
    Schaeffer AJ; Chung J; Heretis K; Wong A; Ledbetter DH; Lese Martin C
    Am J Hum Genet; 2004 Jun; 74(6):1168-74. PubMed ID: 15127362
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genomic changes detected by array CGH in human embryos with developmental defects.
    Rajcan-Separovic E; Qiao Y; Tyson C; Harvard C; Fawcett C; Kalousek D; Stephenson M; Philipp T
    Mol Hum Reprod; 2010 Feb; 16(2):125-34. PubMed ID: 19778950
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples.
    Menten B; Swerts K; Delle Chiaie B; Janssens S; Buysse K; Philippé J; Speleman F
    BMC Med Genet; 2009 Sep; 10():89. PubMed ID: 19751515
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH)-Re-evaluation of chromosome aberration rates in early spontaneous abortions.
    Fritz B; Hallermann C; Olert J; Fuchs B; Bruns M; Aslan M; Schmidt S; Coerdt W; Müntefering H; Rehder H
    Eur J Hum Genet; 2001 Jul; 9(7):539-47. PubMed ID: 11464246
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cytogenetic Analysis of Sporadic First-Trimester Miscarriage Specimens Using Karyotyping and QF-PCR: A Retrospective Romanian Cohort Study.
    Popescu-Hobeanu G; Riza AL; Streață I; Tudorache Ș; Comănescu A; Tănase F; Drăgușin RC; Pascu C; Dijmărescu AL; Cara ML; Dorobanțu Ș; Petre-Mandache B; Cucu M; Sosoi SS; Ioana M; Iliescu D; Burada F
    Genes (Basel); 2022 Nov; 13(12):. PubMed ID: 36553513
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Diagnosis of miscarriages by molecular karyotyping: benefits and pitfalls.
    Robberecht C; Schuddinck V; Fryns JP; Vermeesch JR
    Genet Med; 2009 Sep; 11(9):646-54. PubMed ID: 19617844
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Array comparative genomic hybridization analysis in first-trimester spontaneous abortions with 'normal' karyotypes.
    Shimokawa O; Harada N; Miyake N; Satoh K; Mizuguchi T; Niikawa N; Matsumoto N
    Am J Med Genet A; 2006 Sep; 140(18):1931-5. PubMed ID: 16906550
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. Genetic analysis of first-trimester miscarriages with a combination of cytogenetic karyotyping, microsatellite genotyping and arrayCGH.
    Zhang YX; Zhang YP; Gu Y; Guan FJ; Li SL; Xie JS; Shen Y; Wu BL; Ju W; Jenkins EC; Brown WT; Zhong N
    Clin Genet; 2009 Feb; 75(2):133-40. PubMed ID: 19215247
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chromosomal copy number analysis on chorionic villus samples from early spontaneous miscarriages by high throughput genetic technology.
    Shen J; Wu W; Gao C; Ochin H; Qu D; Xie J; Gao L; Zhou Y; Cui Y; Liu J
    Mol Cytogenet; 2016; 9():7. PubMed ID: 26819630
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An efficient protocol for the detection of chromosomal abnormalities in spontaneous miscarriages or foetal deaths.
    Dória S; Carvalho F; Ramalho C; Lima V; Francisco T; Machado AP; Brandão O; Sousa M; Matias A; Barros A
    Eur J Obstet Gynecol Reprod Biol; 2009 Dec; 147(2):144-50. PubMed ID: 19740589
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A pilot investigation of low-pass genome sequencing identifying site-specific variation in chromosomal mosaicisms by a multiple site sampling approach in first-trimester miscarriages.
    Li Y; Chau MHK; Zhang YX; Zhao Y; Xue S; Li TC; Cao Y; Dong Z; Choy KW; Chung JPW
    Hum Reprod; 2023 Aug; 38(8):1628-1642. PubMed ID: 37218343
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetics of early miscarriage.
    van den Berg MM; van Maarle MC; van Wely M; Goddijn M
    Biochim Biophys Acta; 2012 Dec; 1822(12):1951-9. PubMed ID: 22796359
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Array comparative genomic hybridization profiling analysis reveals deoxyribonucleic acid copy number variations associated with premature ovarian failure.
    Aboura A; Dupas C; Tachdjian G; Portnoï MF; Bourcigaux N; Dewailly D; Frydman R; Fauser B; Ronci-Chaix N; Donadille B; Bouchard P; Christin-Maitre S
    J Clin Endocrinol Metab; 2009 Nov; 94(11):4540-6. PubMed ID: 19837940
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Spectrum of Cytogenomic Abnormalities Revealed by Array Comparative Genomic Hybridization on Products of Conception Culture Failure and Normal Karyotype Samples.
    Zhou Q; Wu SY; Amato K; DiAdamo A; Li P
    J Genet Genomics; 2016 Mar; 43(3):121-31. PubMed ID: 27020032
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.