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Familial Cancer|September 4, 2016
BRCA testing within the Department of Veterans Affairs: concordance with clinical practice guidelinesDanielle S Chun, Brygida Berse, Vickie L Venne, et al.
Familial Cancer|September 14, 2016
Mutational analysis of TP53 gene in Tunisian familial hematological malignancies and sporadic acute leukemia casesWalid Sabri Hamadou, Sawsen Besbes, Violaine Bourdon, et al.
Familial Cancer|August 25, 2016
Do women change their breast cancer mammogram screening behaviour after BRCA1/2 testing?Geneviève Larouche, Jocelyne Chiquette, Sylvie Pelletier, et al.
Familial Cancer|August 31, 2016
A novel germline POLE mutation causes an early onset cancer prone syndrome mimicking constitutional mismatch repair deficiencyKatharina Wimmer, Andreas Beilken, Rainer Nustede, et al.
Familial Cancer|August 28, 2016
Hereditary leiomyomatosis and renal cell cancer syndrome: identification and clinical characterization of a novel mutation in the FH gene in a Colombian familyCarolina Arenas Valencia, Martha Lucia Rodríguez López, Andrea Yimena Cardona Barreto, et al.
Familial Cancer|May 15, 2017
Heightened perception of breast cancer risk in young women at risk of familial breast cancerRachael Glassey, Moira O'Connor, Angela Ives, et al.
Familial Cancer|June 11, 2017
A single visit multidisciplinary model for managing patients with mutations in moderate and high-risk genes in a community practice settingMichael P O'Leary, Bryan S Goldner, Sridevi Abboy, et al.
Familial Cancer|February 9, 2010
Assessment of clinical practices among cancer genetic counselorsDeborah Wham, Thuy Vu, Gayun Chan-Smutko, et al.
Familial Cancer|June 14, 2017
Constitutional mismatch repair deficiency and Lynch syndrome among consecutive Arab Bedouins with colorectal cancer in IsraelNaim Abu Freha, Yaara Leibovici Weissman, Alexander Fich, et al.
Familial Cancer|June 18, 2017
Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countriesAnne Brédart, Jean-Luc Kop, Antonis C Antoniou, et al.
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