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Familial Cancer|November 13, 2023
Functional and phenotypic consequences of an unusual inversion in MSH2Dylan Pelletier, Abhijit Rath, Nelly Sabbaghian, et al.Familial Cancer|August 4, 2023
Combining clinical and molecular characterization of CDH1: a multidisciplinary approach to reclassification of a splicing variantCorrine Fillman, Arravinth Anantharajah, Briana Marmelstein, et al.Familial Cancer|August 12, 2023
PREMM5 distinguishes sporadic from Lynch syndrome-associated MMR-deficient/MSI-high colorectal cancerRenata L Sandoval, Miki Horiguchi, Chinedu Ukaegbu, et al.Familial Cancer|May 29, 2023
Reclassification of two germline DICER1 splicing variants leads to DICER1 syndrome diagnosisMaria Apellaniz-Ruiz, Nelly Sabbaghian, Anne-Laure Chong, et al.Familial Cancer|June 15, 2023
A mosaic pathogenic variant in MSH6 causes MSH6-deficient colorectal and endometrial cancer in a patient classified as suspected Lynch syndrome: a case reportRomy Walker, Mark Clendenning, Jihoon E Joo, et al.Familial Cancer|February 18, 2026
Misinterpreting the results: patient misconceptions about genetic cancer risk after obstetrical carrier screeningAlex Raghunandan, Sonali Iyer, Shayan Dioun, et al.Familial Cancer|May 20, 2026
Why patient organizations are important to improve care for people with Lynch syndromeJurgen SeppenFamilial Cancer|May 22, 2026
Genotypic and phenotypic characteristics of germline TP53 variant carriers: experience from two cancer genetic counseling unitsBeatriz Grau Mirete, Asia Ferrández Arias, Paula Rodríguez Payá, et al.Familial Cancer|May 25, 2026
Association of gestational choriocarcinoma in a mother and Li-Fraumeni syndrome in her child: The result of a single event?Juliette Sallé, Marie-Anne Brundler, Renee Perrier, et al.Familial Cancer|April 5, 2017
All in the family? Communication of cancer survivors with their familiesDeborah J Bowen, Jennifer L Hay, Julie N Harris-Wai, et al.Pageof 151