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Familial Cancer|June 7, 2020
Two cases of somatic STK11 mosaicism in Danish patients with Peutz-Jeghers syndromeAnne Marie Jelsig, Birgitte Bertelsen, Isabel Forss, et al.
Familial Cancer|May 15, 2020
Biallelic NF1 inactivation in high grade serous ovarian cancers from patients with neurofibromatosis type 1Eliza Courtney, Sock Hoai Chan, Shao Tzu Li, et al.
Familial Cancer|May 21, 2020
Women's responses and understanding of polygenic breast cancer risk informationT Yanes, R Kaur, B Meiser, et al.
Familial Cancer|May 9, 2015
Genotype-phenotype analysis of von Hippel-Lindau syndrome in fifteen Indian familiesNarendranath Vikkath, Sindhu Valiyaveedan, Sheela Nampoothiri, et al.
Familial Cancer|May 9, 2015
Birt-Hogg-Dubé syndrome and intracranial vascular pathologiesRahul Kapoor, Alexander I Evins, Diala Steitieh, et al.
Familial Cancer|May 14, 2015
Prevalence and detection of psychosocial problems in cancer genetic counselingW Eijzenga, E M A Bleiker, D E E Hahn, et al.
Familial Cancer|April 24, 2020
Systematic development of a training program for healthcare professionals to improve communication about breast cancer genetic counseling with low health literate patientsJeanine A M van der Giessen, Margreet G E M Ausems, Maria E T C van den Muijsenbergh, et al.
Familial Cancer|May 5, 2020
MLH1 intronic variants mapping to + 5 position of splice donor sites lead to deleterious effects on RNA splicingTamara Alejandra Piñero, Omar Soukarieh, Marion Rolain, et al.
Familial Cancer|May 8, 2004
Intron 4 mutation in APC gene results in splice defect and attenuated FAP phenotypeDeborah W Neklason, Cindy H Solomon, Amy L Dalton, et al.
Familial Cancer|May 8, 2004
Patients' and professionals' opinions of services for people at an increased risk of colorectal cancer: an exploratory qualitative studyTamar Stermer, Shirley Hodgson, Fred Kavalier, et al.
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