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 *

132 related articles for article (PubMed ID: 20425812)

  • 41. 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]  

  • 42. Genomic and genetic variation in E2F transcription factor-1 in men with nonobstructive azoospermia.
    Jorgez CJ; Wilken N; Addai JB; Newberg J; Vangapandu HV; Pastuszak AW; Mukherjee S; Rosenfeld JA; Lipshultz LI; Lamb DJ
    Fertil Steril; 2015 Jan; 103(1):44-52.e1. PubMed ID: 25439843
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Integration of genomic copy number variations and chemotherapy-response biomarkers in pediatric sarcoma.
    Cheng L; Pandya PH; Liu E; Chandra P; Wang L; Murray ME; Carter J; Ferguson M; Saadatzadeh MR; Bijangi-Visheshsaraei K; Marshall M; Li L; Pollok KE; Renbarger JL
    BMC Med Genomics; 2019 Jan; 12(Suppl 1):23. PubMed ID: 30704460
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans.
    Haraksingh RR; Abyzov A; Urban AE
    BMC Genomics; 2017 Apr; 18(1):321. PubMed ID: 28438122
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Array comparative genomic hybridization and fetal congenital heart defects: a systematic review and meta-analysis.
    Jansen FA; Blumenfeld YJ; Fisher A; Cobben JM; Odibo AO; Borrell A; Haak MC
    Ultrasound Obstet Gynecol; 2015 Jan; 45(1):27-35. PubMed ID: 25319878
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Acquirement of DNA copy number variations in non-small cell lung cancer metastasis to the brain.
    Li F; Sun L; Zhang S
    Oncol Rep; 2015 Oct; 34(4):1701-7. PubMed ID: 26259861
    [TBL] [Abstract][Full Text] [Related]  

  • 47. A multi-sample based method for identifying common CNVs in normal human genomic structure using high-resolution aCGH data.
    Park C; Ahn J; Yoon Y; Park S
    PLoS One; 2011; 6(10):e26975. PubMed ID: 22073121
    [TBL] [Abstract][Full Text] [Related]  

  • 48. [Analysis of genomic copy number variations in two unrelated neonates with 8p deletion and duplication associated with congenital heart disease].
    Mei M; Yang L; Zhan G; Wang H; Ma D; Zhou W; Huang G
    Zhonghua Er Ke Za Zhi; 2014 Jun; 52(6):460-3. PubMed ID: 25190168
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Chromosome microarrays in diagnostic testing: interpreting the genomic data.
    Peters GB; Pertile MD
    Methods Mol Biol; 2014; 1168():117-55. PubMed ID: 24870134
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Improved Detection and Characterization of Copy Number Variations Among Diverse Pig Breeds by Array CGH.
    Wang J; Jiang J; Wang H; Kang H; Zhang Q; Liu JF
    G3 (Bethesda); 2015 Apr; 5(6):1253-61. PubMed ID: 25908567
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Next-generation sequencing of duplication CNVs reveals that most are tandem and some create fusion genes at breakpoints.
    Newman S; Hermetz KE; Weckselblatt B; Rudd MK
    Am J Hum Genet; 2015 Feb; 96(2):208-20. PubMed ID: 25640679
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Genomic and clinical characteristics of microduplications in chromosome 17.
    Shchelochkov OA; Cheung SW; Lupski JR
    Am J Med Genet A; 2010 May; 152A(5):1101-10. PubMed ID: 20425816
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Large scale copy number variation (CNV) at 14q12 is associated with the presence of genomic abnormalities in neoplasia.
    Braude I; Vukovic B; Prasad M; Marrano P; Turley S; Barber D; Zielenska M; Squire JA
    BMC Genomics; 2006 Jun; 7():138. PubMed ID: 16756668
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Microdeletion and microduplication syndromes.
    Vissers LE; Stankiewicz P
    Methods Mol Biol; 2012; 838():29-75. PubMed ID: 22228006
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [Genomic abnormalities in children with mental retardation and autism: the use of comparative genomic hybridization in situ (HRCGH) and molecular karyotyping with DNA-microchips (array CGH)].
    Vorsanova SG; Iurov IIu; Kurinnaia OS; Voinova VIu; Iurov IuB
    Zh Nevrol Psikhiatr Im S S Korsakova; 2013; 113(8):46-9. PubMed ID: 24077551
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Refining the Phenotype of Recurrent Rearrangements of Chromosome 16.
    Redaelli S; Maitz S; Crosti F; Sala E; Villa N; Spaccini L; Selicorni A; Rigoldi M; Conconi D; Dalprà L; Roversi G; Bentivegna A
    Int J Mol Sci; 2019 Mar; 20(5):. PubMed ID: 30836598
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Clinical Findings on Chromosome 1 Copy Number Variations.
    Leitão F; Grangeia A; Pinto J; Passas A; Dória S
    Neuropediatrics; 2022 Aug; 53(4):265-273. PubMed ID: 35835157
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Cytogenomic Evaluation of Subjects with Syndromic and Nonsyndromic Conotruncal Heart Defects.
    de Souza KR; Mergener R; Huber J; Campos Pellanda L; Riegel M
    Biomed Res Int; 2015; 2015():401941. PubMed ID: 26137477
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [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]  

  • 60. Comprehensive genome characterization of solitary fibrous tumors using high-resolution array-based comparative genomic hybridization.
    Bertucci F; Bouvier-Labit C; Finetti P; Adélaïde J; Metellus P; Mokhtari K; Decouvelaere AV; Miquel C; Jouvet A; Figarella-Branger D; Pedeutour F; Chaffanet M; Birnbaum D
    Genes Chromosomes Cancer; 2013 Feb; 52(2):156-64. PubMed ID: 23073997
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.