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Whole-Exome Sequencing of Non-Brca1/Brca2 Mutation Carrier Cases at High-Risk for Hereditary Breast/Ovarian Cancer

AuthID
P-00T-8YX

Author(s)

Felicio, PS

Grasel, RS

Campacci, N

de Paula, AE

Galvao, HCR

Torrezan, GT

Sabato, CS

Fernandes, GC

Souza, CP

Michelli, RD

[+2]·

Matsushita, MM

Revil, T

Ragoussis, J

Couch, FJ

Hart, SN

Reis, RM

Melendez, ME

Tonin, PN

Carraro, DM

Palmero, EI

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Document Type

Article in Press

Year published

2020

Published

in HUMAN MUTATION, ISSN: 1059-7794

Volume: 42, Issue: 3, Pages: 290-299 (10)

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Scopus^®

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Publication Identifiers

DOI: 10.1002/humu.24158

SCOPUS: 2-s2.0-85098118054

Wos: WOS:000602693800001

Source Identifiers

ISSN: 1059-7794

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All authors

Name Order	Name	Name Order	Name	Name Order	Name
1	Felicio, PS;	2	Grasel, RS;	3	Campacci, N;
4	de Paula, AE;	5	Galvao, HCR;	6	Torrezan, GT;
7	Sabato, CS;	8	Fernandes, GC;	9	Souza, CP;
10	Michelli, RD;	11	Andrade, CE;	12	Barros, BDD;
13	Matsushita, MM;	14	Revil, T;	15	Ragoussis, J;
16	Couch, FJ;	17	Hart, SN;	18	Reis, RM;
19	Melendez, ME;	20	Tonin, PN;	21	Carraro, DM;
22	Palmero, EI;

Whole-Exome Sequencing of Non-Brca1/Brca2 Mutation Carrier Cases at High-Risk for Hereditary Breast/Ovarian Cancer

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Whole-Exome Sequencing of Non-Brca1/Brca2 Mutation Carrier Cases at High-Risk for Hereditary Breast/Ovarian Cancer

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