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European Journal of Cancer (Oxford, England : 1990)
|
October 11, 2023
Modified study designs to expand treatment options in personalised oncology: a multistakeholder view
Christophe Le Tourneau, Fabrice André, Åslaug Helland, et al.
Nature Communications
|
April 10, 2020
Author Correction: Diagnosis of fusion genes using targeted RNA sequencing
Erin E Heyer, Ira W Deveson, Danson Wooi, et al.
Metabolomics : Official Journal of the Metabolomic Society
|
November 9, 2024
Connecting the changing trace elements spectrum and survival in sarcoma: a pilot study
Laetitia Collet, Philippe Telouk, Francis Albarede, et al.
Human Mutation
|
March 7, 2019
A quantitative model to predict pathogenicity of missense variants in the TP53 gene
Cristina Fortuno, Arcadi Cipponi, Mandy L Ballinger, et al.
Nature Communications
|
March 29, 2019
Diagnosis of fusion genes using targeted RNA sequencing
Erin E Heyer, Ira W Deveson, Danson Wooi, et al.
Eclinicalmedicine
|
April 28, 2025
Genetic predisposition in sarcomas: clinical implications and management
Elizabeth A Connolly, Kjetil Boye, Sylvie Bonvalot, et al.
Patient Education and Counseling
|
November 1, 2020
Family communication about genomic sequencing: A qualitative study with cancer patients and relatives
Amelia K Smit, Nicci Bartley, Megan C Best, et al.
Nature Medicine
|
April 20, 2022
Delivering precision oncology to patients with cancer
Joaquin Mateo, Lotte Steuten, Philippe Aftimos, et al.
The American Journal of Pathology
|
June 24, 2005
Molecular profiling of giant cell tumor of bone and the osteoclastic localization of ligand for receptor activator of nuclear factor kappaB
Teresa Morgan, Gerald J Atkins, Melanie K Trivett, et al.
European Journal of Human Genetics : EJHG
|
March 12, 2022
Preferences for return of germline genome sequencing results for cancer patients and their genetic relatives in a research setting
Megan C Best, Phyllis Butow, Jacqueline Savard, et al.
Page
of 22
Search research articles
Search
Showing results (151-160 of 217) with videos related to
Sort By:
Page
of 22
European Journal of Cancer (Oxford, England : 1990)
|
October 11, 2023
Modified study designs to expand treatment options in personalised oncology: a multistakeholder view
Christophe Le Tourneau, Fabrice André, Åslaug Helland, et al.
Nature Communications
|
April 10, 2020
Author Correction: Diagnosis of fusion genes using targeted RNA sequencing
Erin E Heyer, Ira W Deveson, Danson Wooi, et al.
Metabolomics : Official Journal of the Metabolomic Society
|
November 9, 2024
Connecting the changing trace elements spectrum and survival in sarcoma: a pilot study
Laetitia Collet, Philippe Telouk, Francis Albarede, et al.
Human Mutation
|
March 7, 2019
A quantitative model to predict pathogenicity of missense variants in the TP53 gene
Cristina Fortuno, Arcadi Cipponi, Mandy L Ballinger, et al.
Nature Communications
|
March 29, 2019
Diagnosis of fusion genes using targeted RNA sequencing
Erin E Heyer, Ira W Deveson, Danson Wooi, et al.
Eclinicalmedicine
|
April 28, 2025
Genetic predisposition in sarcomas: clinical implications and management
Elizabeth A Connolly, Kjetil Boye, Sylvie Bonvalot, et al.
Patient Education and Counseling
|
November 1, 2020
Family communication about genomic sequencing: A qualitative study with cancer patients and relatives
Amelia K Smit, Nicci Bartley, Megan C Best, et al.
Nature Medicine
|
April 20, 2022
Delivering precision oncology to patients with cancer
Joaquin Mateo, Lotte Steuten, Philippe Aftimos, et al.
The American Journal of Pathology
|
June 24, 2005
Molecular profiling of giant cell tumor of bone and the osteoclastic localization of ligand for receptor activator of nuclear factor kappaB
Teresa Morgan, Gerald J Atkins, Melanie K Trivett, et al.
European Journal of Human Genetics : EJHG
|
March 12, 2022
Preferences for return of germline genome sequencing results for cancer patients and their genetic relatives in a research setting
Megan C Best, Phyllis Butow, Jacqueline Savard, et al.
Page
of 22