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Hereditary Cancer in Clinical Practice|August 9, 2019
Examining intrafamilial communication of colorectal cancer risk status to family members and kin responses to colonoscopy: a qualitative studyKaitlin M McGarragle, Crystal Hare, Spring Holter, et al.
Hereditary Cancer in Clinical Practice|August 16, 2019
Germline c.1A>C heterozygous pathogenic variant in SDHA reported for the first time in a young adult with a gastric gastrointestinal stromal tumour (GIST): a case reportSergio Carrera, Elena Beristain, Aintzane Sancho, et al.
Hereditary Cancer in Clinical Practice|August 20, 2019
Patient-physician relationships, health self-efficacy, and gynecologic cancer screening among women with Lynch syndromeKaitlin M McGarragle, Melyssa Aronson, Kara Semotiuk, et al.
Hereditary Cancer in Clinical Practice|March 24, 2017
The genetic basis of colonic adenomatous polyposis syndromesBente A Talseth-Palmer
Hereditary Cancer in Clinical Practice|November 3, 2018
A retrospective study of extracolonic, non-endometrial cancer in Swedish Lynch syndrome familiesMasoud Karimi, Jenny von Salomé, Christos Aravidis, et al.
Hereditary Cancer in Clinical Practice|April 10, 2014
A risk of breast cancer in women - carriers of constitutional CHEK2 gene mutations, originating from the North - Central PolandAneta Bąk, Hanna Janiszewska, Anna Junkiert-Czarnecka, et al.
Hereditary Cancer in Clinical Practice|May 13, 2014
The role of Wnt signaling pathway in carcinogenesis and implications for anticancer therapeuticsAsfandyar Sheikh, Asfandyar Khan Niazi, Muhammad Zafar Ahmed, et al.
Hereditary Cancer in Clinical Practice|July 27, 2019
Somatic variants of potential clinical significance in the tumors of BRCA phenocopiesLela Buckingham, Rachel Mitchell, Mark Maienschein-Cline, et al.
Hereditary Cancer in Clinical Practice|March 29, 2019
Selected features of breast and peritoneal cancers diagnosed in BRCA1 carriers after risk-reducing salpingo-oophorectomyJanusz Menkiszak, Anita Chudecka-Głaz, Aneta Cymbaluk-Płoska, et al.
Hereditary Cancer in Clinical Practice|October 24, 2012
Absence of the RET+3:T allele in the MTC patientsPawel Borun, Sowinski Jerzy, Katarzyna Ziemnicka, et al.
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