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Familial Cancer|March 23, 2011
Adequacy of risk-reducing gynaecologic surgery in BRCA1 or BRCA2 mutation carriers and other women at high risk of pelvic serous cancerB E Kiely, M L Friedlander, R L Milne, et al.
Familial Cancer|March 2, 2021
Effective identification of cancer predisposition syndromes in children with cancer employing a questionnaireMiriam Schwermer, Astrid Behnert, Beate Dörgeloh, et al.
Familial Cancer|March 25, 2021
Extended gene panel testing in lobular breast cancerElke M van Veen, D Gareth Evans, Elaine F Harkness, et al.
Familial Cancer|July 20, 2019
TP53 variants of uncertain significance: increasing challenges in variant interpretation and genetic counselingCamila Matzenbacher Bittar, Igor Araujo Vieira, Cristina Silva Sabato, et al.
Familial Cancer|April 15, 2024
Aspects and outcomes of surveillance for individuals at high-risk of pancreatic cancerAleksander M Bogdanski, Jeanin E van Hooft, Bas Boekestijn, et al.
Familial Cancer|August 14, 2014
High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registryChristophe Rosty, Michael D Walsh, Noralane M Lindor, et al.
Familial Cancer|July 12, 2014
Hereditary leiomyomatosis and renal cell cancer (HLRCC): renal cancer risk, surveillance and treatmentFred H Menko, Eamonn R Maher, Laura S Schmidt, et al.
Familial Cancer|August 28, 2014
Association of reduced XRCC2 expression with lymph node metastasis in breast cancer tissuesNabiha Bashir, Syeda Sana, Ishrat Mahjabeen, et al.
Familial Cancer|March 13, 2016
Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancerAryana S Jacobs, Marc D Schwartz, Heiddis Valdimarsdottir, et al.
Familial Cancer|August 13, 2015
The effect of personal medical history and family history of cancer on the uptake of risk-reducing salpingo-oophorectomyJessica E van der Aa, Jacob P Hoogendam, Els S F Butter, et al.
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