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Hereditary Cancer in Clinical Practice|April 14, 2022
Reflex BRCA1 and BRCA2 tumour genetic testing for high-grade serous ovarian cancer: streamlined for clinicians but what do patients think?Jeanna M McCuaig, Sarah E Ferguson, Danielle Vicus, et al.
Hereditary Cancer in Clinical Practice|October 30, 2013
Hereditary cancer risk assessment: essential tools for a better approachIsrael Gomy, Maria Del Pilar Estevez Diz
Hereditary Cancer in Clinical Practice|June 3, 2016
Implications of using whole genome sequencing to test unselected populations for high risk breast cancer genes: a modelling studyCharlotte Warren-Gash, Mark Kroese, Hilary Burton, et al.
Hereditary Cancer in Clinical Practice|August 4, 2017
Preoperative genetic testing impacts surgical decision making in BRCA mutation carriers with breast cancer: a retrospective cohort analysisSiddhartha Yadav, Ashley Reeves, Sarah Campian, et al.
Hereditary Cancer in Clinical Practice|April 19, 2016
Intensive breast screening in BRCA2 mutation carriers is associated with reduced breast cancer specific and all cause mortalityD G Evans, E F Harkness, A Howell, et al.
Hereditary Cancer in Clinical Practice|October 20, 2017
Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database reportToni Seppälä, Kirsi Pylvänäinen, Dafydd Gareth Evans, et al.
Hereditary Cancer in Clinical Practice|July 26, 2019
Age-adjusted association of homologous recombination genes with ovarian cancer using clinical exomes as controlsKevin J Arvai, Maegan E Roberts, Rebecca I Torene, et al.
Hereditary Cancer in Clinical Practice|July 26, 2019
Mutational analysis of BRCA1 and BRCA2 genes in women with familial breast cancer from different regions of ColombiaCarolina Cortés, Ana Lucía Rivera, David Trochez, et al.
Hereditary Cancer in Clinical Practice|February 10, 2021
Characteristics of BRCA1/2 pathogenic germline mutations in chinese NSCLC patients and a comparison with HBOCZheyuan Xu, Yang Wang, Lan Wang, et al.
Hereditary Cancer in Clinical Practice|February 13, 2021
Room for improvement: One third of Lynch syndrome patients presenting for genetic testing in a highly specialised centre in Stockholm already have cancerSophie Walton Bernstedt, Jan Björk, Kaisa Fritzell, et al.
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