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Journal Article
BMC Cancer, ISSN 1471-2407, 2018, Volume 18, Issue 1, pp. 828 - 8
Background: Gene fusion events resulting from chromosomal rearrangements play an important role in initiation of lung adenocarcinoma. The recent association of... 
Biomarker | Next-generation sequencing | Detection | FFPE | Lung cancer | Gene fusions | ADENOCARCINOMA | IN-SITU HYBRIDIZATION | RET FUSIONS | IDENTIFICATION | CANCER | ALK REARRANGEMENT | ONCOLOGY | ROS1 | CELL-LINE | IMMUNOHISTOCHEMISTRY | Adenocarcinoma | Usage | Nucleotide sequencing | Research | Diagnosis | Biological markers | DNA sequencing
Journal Article
Genes, Chromosomes and Cancer, ISSN 1045-2257, 05/2011, Volume 50, Issue 5, pp. 307 - 312
Journal Article
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 05/2014, Volume 32, Issue 15_suppl, pp. e11518 - e11518
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 05/2014, Volume 32, Issue 15_suppl, pp. 1555 - 1555
Journal Article
The Journal of Molecular Diagnostics, ISSN 1525-1578, 07/2018, Volume 20, Issue 4, pp. 512 - 521
Detection of 3′ PMS2 copy-number mutations that cause Lynch syndrome is difficult because of highly homologous pseudogenes. To improve the accuracy and... 
LYNCH SYNDROME | PATHOLOGY | COLOSEQ | GENE | CANCER | DELETIONS | Gene Duplication | Humans | Exons - genetics | DNA Copy Number Variations - genetics | High-Throughput Nucleotide Sequencing - methods | Mutation - genetics | Mismatch Repair Endonuclease PMS2 - genetics | Sequence Homology, Nucleic Acid
Journal Article
Genes, Chromosomes and Cancer, ISSN 1045-2257, 01/2013, Volume 52, Issue 1, pp. 107 - 112
Journal Article