Journal
Hereditary Cancer in Clinical Practice
Publication Date
11-16-2020
Volume
18
Issue
1
First Page
23
Document Type
Open Access Publication
DOI
10.1186/s13053-020-00155-w
Rights and Permissions
Khaddour, K., Fields, R.C., Ansstas, M. et al. Metachronous cutaneous squamous cell carcinoma in a young patient as the only presenting symptom to uncover Lynch syndrome with MLH1 Germline mutation. Hered Cancer Clin Pract 18, 23 (2020). doi.org/10.1186/s13053-020-00155-w This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
Recommended Citation
Khaddour, Karam; Fields, Ryan C; Ansstas, Michael; Rosman, Ilana S; and Ansstas, George, "Metachronous cutaneous squamous cell carcinoma in a young patient as the only presenting symptom to uncover Lynch syndrome with MLH1 germline mutation." Hereditary Cancer in Clinical Practice. 18, 1. 23 (2020).
https://digitalcommons.wustl.edu/open_access_pubs/11892
