Petrova, A., Kanarev, M. A case report of a polymorbid patient with NSCLC harboring an uncommon L861Q EXON 21 EGFR mutation,
, 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. Plovdiv: 28 220-223.