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Familial Cancer|November 15, 2024
The genetic landscape of Lynch syndrome in the Israeli populationAasem Abu Shtaya, Sofia Naftaly Nathan, Inbal Kedar, et al.Familial Cancer|November 15, 2024
BRCAIndica: a resource for ACMG/AMP classified BRCA1 and BRCA2 variantsAastha Vatsyayan, R I Anu, Prerika Mathur, et al.Familial Cancer|October 10, 2024
MSH6-proficient crypt foci in MSH6 constitutional mismatch repair deficiency: reversion of a frameshifted coding microsatellite to its wild-type sequenceJinru Shia, Francisco Sanchez-Vega, Stanley Cho, et al.Familial Cancer|February 18, 2025
CHEK2-related breast cancer: real-world challengesLuiza N Weis, Brittany L Bychkovsky, Adela Rodríguez Hernandez, et al.Familial Cancer|February 7, 2025
Identification of a germline deep intronic PTEN-deletion leading to exonization through whole genome and targeted RNA sequencingMorgane Boedec, Camille Aucouturier, Mathias Cavaillé, et al.Familial Cancer|July 27, 2024
Colonoscopic surveillance in Lynch syndrome: guidelines in perspectiveJoaquín Castillo-Iturra, Ariadna Sánchez, Francesc BalaguerFamilial Cancer|June 21, 2024
Benign tumors and non-melanoma skin cancers in patients with Fanconi anemiaAura Enache, Bia Sajjad, Burak Altintas, et al.Familial Cancer|September 26, 2006
The genetics of FAP and FAP-like syndromesLara Lipton, Ian TomlinsonFamilial Cancer|September 1, 2006
Gastric carcinoid: germline and somatic mutation of the neurofibromatosis type 1 geneW Stewart, J P Traynor, A Cooke, et al.Familial Cancer|September 1, 2006
Molecular diagnosis of neurofibromatosis type 1: 2 years experienceSiân Griffiths, Peter Thompson, Ian Frayling, et al.Pageof 151