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Familial Cancer|July 26, 2012
Novel mutations of OGG1 base excision repair pathway gene in laryngeal cancer patientsIshrat Mahjabeen, Nosheen Masood, Ruqia Mehmood Baig, et al.Familial Cancer|July 7, 2012
Aberrant splicing caused by a MLH1 splice donor site mutation found in a young Japanese patient with Lynch syndromeMasanobu Takahashi, Yoichi Furukawa, Hideki Shimodaira, et al.Familial Cancer|February 11, 2015
Analysis of PALB2 in a cohort of Italian breast cancer patients: identification of a novel PALB2 truncating mutationMaria Teresa Vietri, Gemma Caliendo, Concetta Schiano, et al.Familial Cancer|February 22, 2015
Timing of risk reducing mastectomy in breast cancer patients carrying a BRCA1/2 mutation: retrospective data from the Dutch HEBON studyM R Wevers, M K Schmidt, E G Engelhardt, et al.Familial Cancer|March 1, 2015
The analysis of a large Danish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 11q24Laura Aviaja Rudkjøbing, Hans Eiberg, Hanne Birte Mikkelsen, et al.Familial Cancer|January 25, 2022
Juvenile polyposis diagnosed with an integrated histological, immunohistochemical and molecular approach identifying new SMAD4 pathogenic variantsAndrea Mafficini, Lodewijk A A Brosens, Maria L Piredda, et al.Familial Cancer|April 18, 2019
Genetic counseling referral for ovarian cancer patients: a call to actionChristine Garcia, Kara Harrison, Kari L Ring, et al.Familial Cancer|October 12, 2012
The spectrum of urological malignancy in Lynch syndromeP J Barrow, S Ingham, C O'Hara, et al.Familial Cancer|January 28, 2023
Heritable methylation marks associated with prostate cancer riskJames G Dowty, Chenglong Yu, Mahnaz Hosseinpour, et al.Familial Cancer|February 26, 2025
A novel likely pathogenic germline variant in CDKN1B in a patient with MEN4 and medullary thyroid cancerFernández Mercè, Queralt Asla, Francisco J Illana, et al.Pageof 151