Open AccessAbstract 4871: Whole-exome sequencing identifies a high frequency of germline deleterious variants in cancer predisposition genes in individuals with osteosarcoma
Author(s) -
Roelof Koster,
Bin Zhu,
Meredith Yeager,
Michael Dean,
Matthew Gianferante,
Lei Song,
Joshua N. Sampson,
Julie M. Gastier-Foster,
Richard Görlick,
Sílvia Regina Caminada de Toledo,
Antônio Sérgio Petrilli,
Ana Patiño-Garcı́a,
Fernando Lecanda,
Massimo Serra,
Claudia Maria Hattinger,
Piero Picci,
Katia Scotlandi,
Adrienne M. Flanagan,
Roberto Tirabosco,
Maria Fernanda Amary,
Nilgün Kurucu,
İlhan İnci,
Neriman Sarı,
Mandy L. Ballinger,
David Thomas,
Donald A. Barkauskas,
Belynda Hicks,
Margaret A. Tucker,
Neil Caporaso,
Robert N. Hoover,
Stephen Chanock,
Sharon A. Savage,
Lisa Mirabello
Publication year - 2017
Publication title -
cancer research
Language(s) - English
Resource type - Conference proceedings
eISSN - 1538-7445
pISSN - 0008-5472
DOI - 10.1158/1538-7445.am2017-4871
Subject(s) - exome sequencing , genetics , exome , germline , in silico , biology , cancer , germline mutation , gene , mutation