Identifying patients with Lynch syndrome using a universal tumor screening program in an integrated healthcare system.
- DOI
- 10.1186/s13053-022-00217-1
- Published
- 2022 Apr 18
- Container
- Hereditary cancer in clinical practice
- Publisher
- Not recorded
- Open access
- yes
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limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
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Cite this work
BibTeX
@article{allodium:10.1186/s13053-022-00217-1,
title = {Identifying patients with Lynch syndrome using a universal tumor screening program in an integrated healthcare system.},
author = {Crain PR and Zepp JM and Gille S and Jenkins L and Kauffman TL and Shuster E and Goddard KAB and Wilfond BS and Hunter JE},
year = {2022},
journal = {Hereditary cancer in clinical practice},
doi = {10.1186/s13053-022-00217-1},
url = {https://doi.org/10.1186/s13053-022-00217-1}
}RIS
TY - JOUR TI - Identifying patients with Lynch syndrome using a universal tumor screening program in an integrated healthcare system. AU - Crain PR AU - Zepp JM AU - Gille S AU - Jenkins L AU - Kauffman TL AU - Shuster E AU - Goddard KAB AU - Wilfond BS AU - Hunter JE PY - 2022 JO - Hereditary cancer in clinical practice DO - 10.1186/s13053-022-00217-1 UR - https://doi.org/10.1186/s13053-022-00217-1 ER -
APA
PR, C., JM, Z., S, G., L, J., TL, K., E, S., KAB, G., BS, W., & JE, H. (2022). Identifying patients with Lynch syndrome using a universal tumor screening program in an integrated healthcare system.. Hereditary cancer in clinical practice. https://doi.org/10.1186/s13053-022-00217-1
Source records
- pubmed · retrieved 2026-09-25T21:27:34.774Z