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The Lancet. Oncology
|
December 17, 2008
Familial cancer database online
Irene Rainville, Judy E Garber
Abdominal Imaging
|
May 15, 2012
Synchronous small bowel and atypical primary leiomyosarcoma of inferior vena cava in a patient with RB1 mutation
Sachin S Saboo, Nikhil Ramaiya, Heather Jacene, et al.
Cancer Genetics
|
October 15, 2023
Breast and colorectal cancer risks among over 6,000 CHEK2 pathogenic variant carriers: A comparison of missense versus truncating variants
Erin Mundt, Brent Mabey, Irene Rainville, et al.
Breast Cancer Research and Treatment
|
January 30, 2020
High risk of breast cancer in women with biallelic pathogenic variants in CHEK2
Irene Rainville, Shanell Hatcher, Eric Rosenthal, et al.
Acta Gastroenterologica Latinoamericana
|
May 23, 2014
Dysphagia, melanosis, gastrointestinal stromal tumors and a germinal mutation of the KIT gene in an Argentine family
Silvia Adela Avila, José Peñaloza, Flavia González, et al.
European Journal of Endocrinology
|
August 19, 2017
Adrenocortical carcinoma and succinate dehydrogenase gene mutations: an observational case series
Tobias Else, Antonio Marcondes Lerario, Jessica Everett, et al.
Cancer
|
June 14, 2017
The association between germline BRCA2 variants and sensitivity to platinum-based chemotherapy among men with metastatic prostate cancer
Mark M Pomerantz, Sandor Spisák, Li Jia, et al.
Blood
|
February 24, 2016
Exome sequencing reveals recurrent germ line variants in patients with familial Waldenström macroglobulinemia
Aldo M Roccaro, Antonio Sacco, Jiantao Shi, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
August 14, 2023
Germline <i>EGFR</i> Mutations and Familial Lung Cancer
Geoffrey R Oxnard, Ruthia Chen, Jennifer C Pharr, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
The Lancet. Oncology
|
December 17, 2008
Familial cancer database online
Irene Rainville, Judy E Garber
Abdominal Imaging
|
May 15, 2012
Synchronous small bowel and atypical primary leiomyosarcoma of inferior vena cava in a patient with RB1 mutation
Sachin S Saboo, Nikhil Ramaiya, Heather Jacene, et al.
Cancer Genetics
|
October 15, 2023
Breast and colorectal cancer risks among over 6,000 CHEK2 pathogenic variant carriers: A comparison of missense versus truncating variants
Erin Mundt, Brent Mabey, Irene Rainville, et al.
Breast Cancer Research and Treatment
|
January 30, 2020
High risk of breast cancer in women with biallelic pathogenic variants in CHEK2
Irene Rainville, Shanell Hatcher, Eric Rosenthal, et al.
Acta Gastroenterologica Latinoamericana
|
May 23, 2014
Dysphagia, melanosis, gastrointestinal stromal tumors and a germinal mutation of the KIT gene in an Argentine family
Silvia Adela Avila, José Peñaloza, Flavia González, et al.
European Journal of Endocrinology
|
August 19, 2017
Adrenocortical carcinoma and succinate dehydrogenase gene mutations: an observational case series
Tobias Else, Antonio Marcondes Lerario, Jessica Everett, et al.
Cancer
|
June 14, 2017
The association between germline BRCA2 variants and sensitivity to platinum-based chemotherapy among men with metastatic prostate cancer
Mark M Pomerantz, Sandor Spisák, Li Jia, et al.
Blood
|
February 24, 2016
Exome sequencing reveals recurrent germ line variants in patients with familial Waldenström macroglobulinemia
Aldo M Roccaro, Antonio Sacco, Jiantao Shi, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
August 14, 2023
Germline <i>EGFR</i> Mutations and Familial Lung Cancer
Geoffrey R Oxnard, Ruthia Chen, Jennifer C Pharr, et al.
Page
of 1