Petrova, A., Kanarev, M. A case report of a polymorbid patient with NSCLC harboring an uncommon L861Q EXON 21 EGFR mutation. Plovdiv: 2022 220-223,.
Petrova, A., Kanarev, M. A case report of a polymorbid patient with NSCLC harboring an uncommon L861Q EXON 21 EGFR mutation. Plovdiv: 2022 220-223,.
Petrova, A., Kanarev, M. (2022) A case report of a polymorbid patient with NSCLC harboring an uncommon L861Q EXON 21 EGFR mutation, Plovdiv: 220-223,.
Petrova, A., & Kanarev, M. (2022). A case report of a polymorbid patient with NSCLC harboring an uncommon L861Q EXON 21 EGFR mutation. Scientific Works of the Union of Scientists in Bulgaria - Plovdiv. Series G. Medicine, Pharmacy and Dental Medicine, 28 220-223.
Petrova A, Kanarev M. A case report of a polymorbid patient with NSCLC harboring an uncommon L861Q EXON 21 EGFR mutation. Scientific Works of the Union of Scientists in Bulgaria - Plovdiv. Series G. Medicine, Pharmacy and Dental Medicine. 2022; 28: 220-223.
