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Familial Cancer|October 11, 2018
Risk of multiple colorectal cancer development depends on age and subgroup in individuals with hereditary predispositionLars J Lindberg, Wia Wegen-Haitsma, Steen Ladelund, et al.
Familial Cancer|October 11, 2018
Boosting care and knowledge about hereditary cancer: European Reference Network on Genetic Tumour Risk SyndromesJanet R Vos, Lisette Giepmans, Claas Röhl, et al.
Familial Cancer|January 6, 2018
Gene expression analysis in peripheral blood cells of patients with hereditary leiomyomatosis and renal cell cancer syndrome (HLRCC): identification of NRF2 pathway activationCarolina Arenas Valencia, Liliana Lopez Kleine, Andres M Pinzon Velasco, et al.
Familial Cancer|March 19, 2018
Clinical and pathologic characteristics of breast cancer patients carrying the c.3481_3491del11 mutationR El Tannouri, E Albuisson, P Jonveaux, et al.
Familial Cancer|January 6, 2021
Atypical choroidal nevus in a subject with a germline PALB2 pathogenic variantTimothy W Grosel, Matthew Karl, Robert T Pilarski, et al.
Familial Cancer|January 7, 2021
Genetic evaluation of patients and families with concern for hereditary endocrine tumor syndromesJennifer L Anderson, Robert Pilarski, Lawrence Kirschner, et al.
Familial Cancer|February 24, 2020
Increased prevalence of Barrett's esophagus in patients with MUTYH-associated polyposis (MAP)Ceranza G Daans, Zeinab Ghorbanoghli, Mary E Velthuizen, et al.
Familial Cancer|February 14, 2020
Novel intronic variant in PALB2 gene and effective prevention of Fanconi anemia in familyI Viakhireva, E Musatova, L Bessonova, et al.
Familial Cancer|February 29, 2020
Do the risks of Lynch syndrome-related cancers depend on the parent of origin of the mutation?Shimelis Dejene Gemechu, Christine M van Vliet, Aung Ko Win, et al.
Familial Cancer|February 1, 2020
Mainstreamed genetic testing of breast cancer patients in two hospitals in South Eastern NorwayEli Marie Grindedal, Kjersti Jørgensen, Pernilla Olsson, et al.
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