Moving precision forward: extending next generation sequencing to operable disease in less common breast cancer subtypes.
Publication
, Journal Article
Thomas, A; Shatsky, R; Kalinsky, K
Published in: Ann Oncol
January 2024
Duke Scholars
Published In
Ann Oncol
DOI
EISSN
1569-8041
Publication Date
January 2024
Volume
35
Issue
1
Start / End Page
7 / 9
Location
England
Related Subject Headings
- Receptor, erbB-2
- Receptor, ErbB-2
- Oncology & Carcinogenesis
- Mutation
- Humans
- High-Throughput Nucleotide Sequencing
- Female
- Breast Neoplasms
- 3211 Oncology and carcinogenesis
- 3202 Clinical sciences
Citation
APA
Chicago
ICMJE
MLA
NLM
Thomas, A., Shatsky, R., & Kalinsky, K. (2024). Moving precision forward: extending next generation sequencing to operable disease in less common breast cancer subtypes. Ann Oncol, 35(1), 7–9. https://doi.org/10.1016/j.annonc.2023.10.127
Thomas, A., R. Shatsky, and K. Kalinsky. “Moving precision forward: extending next generation sequencing to operable disease in less common breast cancer subtypes.” Ann Oncol 35, no. 1 (January 2024): 7–9. https://doi.org/10.1016/j.annonc.2023.10.127.
Thomas A, Shatsky R, Kalinsky K. Moving precision forward: extending next generation sequencing to operable disease in less common breast cancer subtypes. Ann Oncol. 2024 Jan;35(1):7–9.
Thomas, A., et al. “Moving precision forward: extending next generation sequencing to operable disease in less common breast cancer subtypes.” Ann Oncol, vol. 35, no. 1, Jan. 2024, pp. 7–9. Pubmed, doi:10.1016/j.annonc.2023.10.127.
Thomas A, Shatsky R, Kalinsky K. Moving precision forward: extending next generation sequencing to operable disease in less common breast cancer subtypes. Ann Oncol. 2024 Jan;35(1):7–9.
Published In
Ann Oncol
DOI
EISSN
1569-8041
Publication Date
January 2024
Volume
35
Issue
1
Start / End Page
7 / 9
Location
England
Related Subject Headings
- Receptor, erbB-2
- Receptor, ErbB-2
- Oncology & Carcinogenesis
- Mutation
- Humans
- High-Throughput Nucleotide Sequencing
- Female
- Breast Neoplasms
- 3211 Oncology and carcinogenesis
- 3202 Clinical sciences