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European Journal of Human Genetics : EJHG
|
January 5, 2022
Multilocus Inherited Neoplasia Allele Syndrome (MINAS): an update
Anthony McGuigan, James Whitworth, Avgi Andreou, et al.
Journal of Medical Genetics
|
April 10, 2025
Economic evaluation of personalised versus conventional risk assessment for women who have undergone testing for hereditary breast and ovarian cancer genes: a modelling study
Qin Xi, Nichola Fennell, Stephanie Archer, et al.
European Journal of Medical Genetics
|
October 4, 2021
Overview of hereditary breast and ovarian cancer (HBOC) guidelines across Europe
David Humberto Marmolejo, Mark Yu Zheng Wong, Svetlana Bajalica-Lagercrantz, et al.
Journal of Neuropathology and Experimental Neurology
|
March 11, 2015
Malignant peripheral nerve sheath tumor in cowden syndrome: a first report
Amy Taylor, Isabelle Delon, Kieren Allinson, et al.
Familial Cancer
|
August 9, 2011
Acinic cell carcinoma of the retromolar trigone region: expanding the tumor phenotype in Cowden syndrome?
Hugo Villeneuve, Steve Tremblay, Polymnia Galiatsatos, et al.
Journal of Medical Genetics
|
November 22, 2013
Fanconi anaemia, BRCA2 mutations and childhood cancer: a developmental perspective from clinical and epidemiological observations with implications for genetic counselling
Stefan Meyer, Marc Tischkowitz, Kate Chandler, et al.
European Journal of Medical Genetics
|
September 11, 2024
Economic evaluation of extended panel analysis in cancer patients with historical NHS diagnostic germline genetic testing - A modeling study based on real-world data
Qin Xi, Rahul Patel, Thomas Linton-Willoughby, et al.
Breast Cancer Research and Treatment
|
August 13, 2008
Analysis of the genes coding for the BRCA1-interacting proteins, RAP80 and Abraxas (CCDC98), in high-risk, non-BRCA1/2, multiethnic breast cancer cases
David J Novak, Nelly Sabbaghian, Philippe Maillet, et al.
Journal of Medical Genetics
|
April 18, 2018
Consensus for genes to be included on cancer panel tests offered by UK genetics services: guidelines of the UK Cancer Genetics Group
Amy Taylor, Angela F Brady, Ian M Frayling, et al.
The Prostate
|
February 22, 2008
Analysis of the gene coding for the BRCA2-interacting protein PALB2 in hereditary prostate cancer
Marc Tischkowitz, Nelly Sabbaghian, Anna M Ray, et al.
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of 26
Search research articles
Search
Showing results (21-30 of 258) with videos related to
Sort By:
Page
of 26
European Journal of Human Genetics : EJHG
|
January 5, 2022
Multilocus Inherited Neoplasia Allele Syndrome (MINAS): an update
Anthony McGuigan, James Whitworth, Avgi Andreou, et al.
Journal of Medical Genetics
|
April 10, 2025
Economic evaluation of personalised versus conventional risk assessment for women who have undergone testing for hereditary breast and ovarian cancer genes: a modelling study
Qin Xi, Nichola Fennell, Stephanie Archer, et al.
European Journal of Medical Genetics
|
October 4, 2021
Overview of hereditary breast and ovarian cancer (HBOC) guidelines across Europe
David Humberto Marmolejo, Mark Yu Zheng Wong, Svetlana Bajalica-Lagercrantz, et al.
Journal of Neuropathology and Experimental Neurology
|
March 11, 2015
Malignant peripheral nerve sheath tumor in cowden syndrome: a first report
Amy Taylor, Isabelle Delon, Kieren Allinson, et al.
Familial Cancer
|
August 9, 2011
Acinic cell carcinoma of the retromolar trigone region: expanding the tumor phenotype in Cowden syndrome?
Hugo Villeneuve, Steve Tremblay, Polymnia Galiatsatos, et al.
Journal of Medical Genetics
|
November 22, 2013
Fanconi anaemia, BRCA2 mutations and childhood cancer: a developmental perspective from clinical and epidemiological observations with implications for genetic counselling
Stefan Meyer, Marc Tischkowitz, Kate Chandler, et al.
European Journal of Medical Genetics
|
September 11, 2024
Economic evaluation of extended panel analysis in cancer patients with historical NHS diagnostic germline genetic testing - A modeling study based on real-world data
Qin Xi, Rahul Patel, Thomas Linton-Willoughby, et al.
Breast Cancer Research and Treatment
|
August 13, 2008
Analysis of the genes coding for the BRCA1-interacting proteins, RAP80 and Abraxas (CCDC98), in high-risk, non-BRCA1/2, multiethnic breast cancer cases
David J Novak, Nelly Sabbaghian, Philippe Maillet, et al.
Journal of Medical Genetics
|
April 18, 2018
Consensus for genes to be included on cancer panel tests offered by UK genetics services: guidelines of the UK Cancer Genetics Group
Amy Taylor, Angela F Brady, Ian M Frayling, et al.
The Prostate
|
February 22, 2008
Analysis of the gene coding for the BRCA2-interacting protein PALB2 in hereditary prostate cancer
Marc Tischkowitz, Nelly Sabbaghian, Anna M Ray, et al.
Page
of 26