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Familial Cancer|September 7, 2015
Rhabdoid tumor predisposition syndrome caused by SMARCB1 constitutional deletion: prenatal detection of new case of recurrence in siblings due to gonadal mosaicismLaura Gigante, Irene Paganini, Marina Frontali, et al.Familial Cancer|September 10, 2015
Screening of HELQ in breast and ovarian cancer familiesLiisa M Pelttari, Laura Kinnunen, Johanna I Kiiski, et al.Familial Cancer|January 8, 2015
The breast cancer immunophenotype of TP53-p.R337H carriers is different from that observed among other pathogenic TP53 mutation carriersMariana Fitarelli-Kiehl, Juliana Giacomazzi, Patricia Santos-Silva, et al.Familial Cancer|September 21, 2015
First report of somatic mosaicism for mutations in STK11 in four patients with Peutz-Jeghers syndromeVictoria McKay, Diane Cairns, David Gokhale, et al.Familial Cancer|January 14, 2016
CDH1 germline mutations and hereditary lobular breast cancerGiovanni Corso, Mattia Intra, Chiara Trentin, et al.Familial Cancer|January 11, 2016
Germline BAP1 mutations misreported as somatic based on tumor-only testingMohamed H Abdel-Rahman, Karan Rai, Robert Pilarski, et al.Familial Cancer|December 19, 2015
Determining the familial risk distribution of colorectal cancer: a data mining approachRowena Chau, Mark A Jenkins, Daniel D Buchanan, et al.Familial Cancer|February 3, 2016
Migrant breast cancer patients and their participation in genetic counseling: results from a registry-based studyJ E Baars, A M van Dulmen, M E Velthuizen, et al.Familial Cancer|October 10, 2015
Surveillance using capsule endoscopy is safe in post-colectomy patients with familial adenomatous polyposis: a prospective Japanese studyMinori Matsumoto, Takeshi Nakajima, Yasuo Kakugawa, et al.Familial Cancer|November 7, 2014
Estimate of the penetrance of BRCA mutation and the COS software for the assessment of BRCA mutation probabilityJacopo Berrino, Franco Berrino, Silvia Francisci, et al.Pageof 151