作者: Christine Sers , Jürgen R. Fischer , Michael Thomas , Felix J. F. Herth , Manfred Dietel
DOI: 10.1007/S00428-012-1219-X
关键词: Sanger sequencing 、 Biopsy 、 Mutation testing 、 Algorithm 、 Pulmonary adenocarcinoma 、 Egfr mutation 、 Biology 、 Carcinoma 、 Tyrosine-kinase inhibitor 、 Mutational status
摘要: … Based on the determined detection limit for EGFR mutations by Sanger sequencing we aimed to develop an algorithm for performing and reporting diagnostic analysis of NSCLC …