Germline sequencing identifies rare variants in Finnish subjects with familial germ cell tumors

Authors

Erin L Crowgey, Nemours Alfred I. duPont Hospital for Children
Tea Soini, University of Helsinki
Nidhi Shah, Nemours Alfred I. duPont Hospital for Children
Satu-Liisa Pauniaho, University of Helsinki
Pekka Lahdenne, University of Helsinki
David B Wilson, Washington University School of Medicine in St. Louis
Markku Heikinheimo, Washington University School of Medicine in St. Louis
Todd E Druley, Washington University School of Medicine in St. Louis

Journal

The Application of Clinical Genetics

Publication Date

2020

Volume

13

First Page

127

Last Page

137

Document Type

Open Access Publication

DOI

10.2147/TACG.S245093

Rights and Permissions

Crowgey EL, Soini T, Shah N, et al. Germline Sequencing Identifies Rare Variants in Finnish Subjects with Familial Germ Cell Tumors. The Application of Clinical Genetics. 2020;13:127-137. https://doi.org/10.2147/TACG.S245093

Recommended Citation

Crowgey, Erin L; Soini, Tea; Shah, Nidhi; Pauniaho, Satu-Liisa; Lahdenne, Pekka; Wilson, David B; Heikinheimo, Markku; and Druley, Todd E, "Germline sequencing identifies rare variants in Finnish subjects with familial germ cell tumors." The Application of Clinical Genetics. 13, 127 - 137. (2020).
https://digitalcommons.wustl.edu/open_access_pubs/9556