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Hereditary Cancer in Clinical Practice|January 26, 2016
Prognostic factors in Polish patients with BRCA1-dependent ovarian cancerWiktor Szatkowski, Paweł Blecharz, Jerzy W Mituś, et al.Hereditary Cancer in Clinical Practice|January 19, 2016
BRCA1 founder mutations do not contribute to increased risk of gastric cancer in the Polish populationMałgorzata Ławniczak, Anna Jakubowska, Andrzej Białek, et al.Hereditary Cancer in Clinical Practice|October 16, 2015
The frequency of BRCA1 founder mutation c.5266dupC (5382insC) in breast cancer patients from UkraineIelizaveta Gorodetska, Svitlana Serga, Natalia Levkovich, et al.Hereditary Cancer in Clinical Practice|June 10, 2016
Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patientsMarc Bennedbæk, Maria Rossing, Åse K Rasmussen, et al.Hereditary Cancer in Clinical Practice|May 31, 2019
Diagnostic mRNA splicing assay for variants in BRCA1 and BRCA2 identified two novel pathogenic splicing aberrationsTeresia Wangensteen, Caroline Nangota Felde, Deeqa Ahmed, et al.Hereditary Cancer in Clinical Practice|August 2, 2018
CD36 - a plausible modifier of disease phenotype in familial adenomatous polyposisMerran Holmes, Toni Connor, Christopher Oldmeadow, et al.Hereditary Cancer in Clinical Practice|April 10, 2019
Increased breast cancer risk in women with neurofibromatosis type 1: a meta-analysis and systematic review of the literatureLorena P Suarez-Kelly, Lianbo Yu, David Kline, et al.Hereditary Cancer in Clinical Practice|October 21, 2021
Unusual course of disease and genetic profile in Li-Fraumeni syndrome-associated osteosarcoma - a case reportAlexander Puzik, Markus Uhl, Juri Ruf, et al.Hereditary Cancer in Clinical Practice|May 5, 2022
Lynch syndrome testing of colorectal cancer patients in a high-income country with universal healthcare: a retrospective study of current practice and gaps in seven australian hospitalsJulia Steinberg, Priscilla Chan, Emily Hogden, et al.Hereditary Cancer in Clinical Practice|February 1, 2022
CHEK2 mutations and papillary thyroid cancer: correlation or coincidence?Kortbeek Koen, De Putter Robin, Naert ElinePageof 48