Complex mutations & subpopulations of deletions at exon 19 of EGFR in NSCLC revealed by next generation sequencing: potential clinical implications.

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作者： Antonio,Marchetti ^[1] ; Maela,Del Grammastro ; Giampaolo,Filice ; Lara,Felicioni ; Giulio,Rossi ; Paolo,Graziano ; Giuliana,Sartori ; Alvaro,Leone ; Sara,Malatesta ; Michele,Iacono ; Luigi,Guetti ; Patrizia,Viola ; Felice,Mucilli ; Franco,Cuccurullo ; Fiamma,Buttitta

作者单位： Center of Predictive Molecular Medicine, University-Foundation, Chieti, Italy. amarchetti@unich.it ^[1]

主题词碱基序列(Base Sequence);癌, 非小细胞肺(Carcinoma, Non-Small-Cell Lung);外显子(Exons);基因缺失(Gene Deletion);基因, erbB-1(Genes, erbB-1);高通量核苷酸序列分析(High-Throughput Nucleotide Sequencing);人类(Humans);肺肿瘤(Lung Neoplasms);分子序列数据(Molecular Sequence Data)

DOI 10.1371/journal.pone.0042164

PMID 22848739

发布时间 2024-11-03

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PloS one

2012年7卷7期

e42164页

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Complex mutations & subpopulations of deletions at exon 19 of EGFR in NSCLC revealed by next generation sequencing: potential clinical implications.

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Complex mutations &amp; subpopulations of deletions at exon 19 of EGFR in NSCLC revealed by next generation sequencing: potential clinical implications.

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Complex mutations & subpopulations of deletions at exon 19 of EGFR in NSCLC revealed by next generation sequencing: potential clinical implications.