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Hereditary Cancer in Clinical Practice|September 17, 2014
Mutation analysis of PALB2 in BRCA1 and BRCA2-negative breast and/or ovarian cancer families from Eastern Ontario, CanadaTaila Hartley, Luca Cavallone, Nelly Sabbaghian, et al.
Hereditary Cancer in Clinical Practice|December 31, 2013
The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patientsBente A Talseth-Palmer, Juul T Wijnen, Eva K Andreassen, et al.
Hereditary Cancer in Clinical Practice|December 24, 2013
The impact of genetic variants in inflammatory-related genes on prostate cancer risk among men of African Descent: a case control studyDominique Z Jones, Camille Ragin, Nayla C Kidd, et al.
Hereditary Cancer in Clinical Practice|April 22, 2016
PALB2: research reaching to clinical outcomes for women with breast cancerMelissa C Southey, Ingrid Winship, Tú Nguyen-Dumont
Hereditary Cancer in Clinical Practice|October 13, 2017
The potential role of miRNAs in therapy of breast and ovarian cancers associated with BRCA1 mutationAgnieszka Strumidło, Sylwia Skiba, Rodney J Scott, et al.
Hereditary Cancer in Clinical Practice|July 15, 2016
A novel deleterious c.2656G>T MSH2 germline mutation in a Pakistani family with a phenotypic overlap of hereditary breast and ovarian cancer and Lynch syndromeMuhammad U Rashid, Humaira Naeemi, Noor Muhammad, et al.
Hereditary Cancer in Clinical Practice|February 18, 2016
When is a mutation not a mutation: the case of the c.594-2A>C splice variant in a woman harbouring another BRCA1 mutation in transMichelle Wong-Brown, Mary McPhillips, Margaret Gleeson, et al.
Hereditary Cancer in Clinical Practice|March 2, 2018
Frequency of BRCA1 and BRCA2 causative founder variants in ovarian cancer patients in South-East PolandTomasz Kluz, Andrzej Jasiewicz, Elżbieta Marczyk, et al.
Hereditary Cancer in Clinical Practice|October 24, 2013
Familial adenomatous polyposis of the colonAndrzej Plawski, Tomasz Banasiewicz, Pawel Borun, et al.
Hereditary Cancer in Clinical Practice|May 17, 2017
A case report of Muir-Torre syndrome in a woman with breast cancer and MSI-Low skin squamous cell carcinomaCaroline Kientz, Marie-Odile Joly, Laurence Faivre, et al.
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