Showing results (831-840 of 1,503) with videos related to
Sort By:
Pageof 151
Familial Cancer|May 8, 2007
Absence of the common IGF1 19 CA-repeat allele is more common among BRCA1 mutation carriers than among non-carriers from BRCA1 familiesMaria Henningson, Erika Bågeman, Therese Sandberg, et al.Familial Cancer|June 8, 2022
A large family with MSH3-related polyposisArthur S Aelvoet, Daniël R Hoekman, Bert J W Redeker, et al.Familial Cancer|November 29, 2022
A PMS2 non-canonical splicing site variant leads to aberrant splicing in a patient suspected for lynch syndromeAhmed Bouras, Pierre Naibo, Clémentine Legrand, et al.Familial Cancer|November 23, 2022
Characterization of sebaceous and non-sebaceous cutaneous manifestations in patients with lynch syndrome: a systematic reviewShahram Aziz, Hazel O'Sullivan, Kara Heelan, et al.Familial Cancer|January 18, 2023
Evaluating the role of CHEK2 p.(Asp438Tyr) allele in inherited breast cancer predispositionTimo A Kumpula, Susanna Koivuluoma, Leila Soikkonen, et al.Familial Cancer|June 14, 2021
First international workshop of the ATM and cancer risk group (4-5 December 2019)Fabienne Lesueur, Douglas F Easton, Anne-Laure Renault, et al.Familial Cancer|October 9, 2017
Whole body magnetic resonance imaging (WB-MRI) and brain MRI baseline surveillance in TP53 germline mutation carriers: experience from the Li-Fraumeni Syndrome Education and Early Detection (LEAD) clinicJasmina Bojadzieva, Behrang Amini, Suzanne F Day, et al.Familial Cancer|October 12, 2017
Family history influences the tumor characteristics and prognosis of breast cancers developing during postmenopausal hormone therapyRainer Fagerholm, Maria Faltinova, Kirsi Aaltonen, et al.Pageof 151