Showing results (11-20 of 473) with videos related to
Sort By:
Pageof 48
Hereditary Cancer in Clinical Practice|May 11, 2018
Retraction Note to: The BRCA2 variant c.68-7 T > A is associated with breast cancerPål Møller, Eivind HovigHereditary Cancer in Clinical Practice|December 9, 2023
SMAD4 variants and its genotype-phenotype correlations to juvenile polyposis syndromeKimberley Cao, John-Paul Plazzer, Finlay MacraeHereditary Cancer in Clinical Practice|August 11, 2023
Factors affecting adherence to a high-risk surveillance protocol among patients with Li-Fraumeni syndromeKaylee A Underkofler, Martha H Thomas, Christina J Taylor, et al.Hereditary Cancer in Clinical Practice|July 17, 2023
Using a multistep approach with multidisciplinary team to increase the diagnosis rate of Lynch syndrome-associated colorectal cancer after universal screening: a single-center study in JapanKyota Tatsuta, Mayu Sakata, Moriya Iwaizumi, et al.Hereditary Cancer in Clinical Practice|July 14, 2023
Lynch-like syndrome with germline WRN mutation in Bulgarian patient with synchronous endometrial and ovarian cancerZornitsa Bogomilova Kamburova, Polina Damyanova Dimitrova, Diana Strateva Dimitrova, et al.Hereditary Cancer in Clinical Practice|September 18, 2020
Public support for healthcare-mediated disclosure of hereditary cancer risk information: Results from a population-based survey in SwedenAndreas Andersson, Carolina Hawranek, Anna Öfverholm, et al.Hereditary Cancer in Clinical Practice|March 4, 2020
Ubiquitous neurocognitive dysfunction in familial adenomatous polyposis: proof-of-concept of the role of APC protein in neurocognitive functionMarcia Roxana Cruz-Correa, Ana Cecilia Sala, Beatriz Cintrón, et al.Hereditary Cancer in Clinical Practice|March 20, 2020
The Prospective Lynch Syndrome Database reports enable evidence-based personal precision health carePål MøllerHereditary Cancer in Clinical Practice|December 9, 2020
Metachronous cutaneous squamous cell carcinoma in a young patient as the only presenting symptom to uncover Lynch syndrome with MLH1 Germline mutationKaram Khaddour, Ryan C Fields, Michael Ansstas, et al.Hereditary Cancer in Clinical Practice|January 5, 2022
Germline HOXB13 mutation p.G84E do not confer an increased bladder or kidney cancer risk in polish populationElżbieta Złowocka-Perłowska, Aleksandra Tołoczko-Grabarek, Jan LubińskiPageof 48