Germline Sequencing Identifies Rare Variants in Finnish Subjects with Familial Germ Cell Tumors

Germline Sequencing Identifies Rare Variants in Finnish Subjects with Familial Germ Cell Tumors

Erin L Crowgey,1 Tea Soini,2 Nidhi Shah,1 Satu-Liisa Pauniaho,2,3 Pekka Lahdenne,2 David B Wilson,4 Markku Heikinheimo,2,4 Todd E Druley4 1Nemours Center for Cancer and Blood Disorders, Nemours Alfred I. duPont Hospital for Children, Wilmington, DE, USA; 2Pediatric Research Center, Children&rsqu...

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Bibliographic Details
Main Authors: Crowgey EL, Soini T, Shah N, Pauniaho SL, Lahdenne P, Wilson DB, Heikinheimo M, Druley TE
Format: Article
Language:English
Published: Dove Medical Press 2020-06-01
Series:The Application of Clinical Genetics
Subjects:
genomics
familial germ cell tumors
next generation sequencing
germline analysis
Online Access:https://www.dovepress.com/germline-sequencing-identifies-rare-variants-in-finnish-subjects-with--peer-reviewed-article-TACG

Internet

https://www.dovepress.com/germline-sequencing-identifies-rare-variants-in-finnish-subjects-with--peer-reviewed-article-TACG

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