Detection of rare single nucleotide variants affecting genes in the DNA repair pathways in hereditary breast cancer

BMC Genomics

Poster Presentation

Adel M. Abuzenadah¹  Adeel G. Chaudhary¹  Shireen Hussein¹  Mamdooh A. Gari¹  Ashraf Dallol¹  Mohammed H. Al-Qahtani¹  Ibtessam R. Hussein¹  Taha Kumosani²  Shadi Al-Khayyat³  Jaudah Al-Maghrabi⁴  Hanaa Tashkandi⁵  Fatma Al-Thubaiti⁵  Adnan Merdad⁵ 

[1] Center of Excellence in Genomic Medicine Research, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia;Department of Biochemistry, Faculty of Science, King Abdulaziz University, Kingdom of Saudi Arabia;Department of Oncology, King Abdulaziz University Hospital, Kingdom of Saudi Arabia;Department of Pathology, King Abdulaziz University Hospital, Kingdom of Saudi Arabia;Department of Surgery, King Abdulaziz University Hospital, Kingdom of Saudi Arabia;

关键词: Breast Cancer;    Breast Cancer Patient;    Positive Family History;    Personalized Medicine;    Exome Sequencing;   

DOI  :  10.1186/1471-2164-15-S2-P20

来源: Springer

【 授权许可】

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© Hussein et al; licensee BioMed Central Ltd. 2014. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.