Cancer genetics program: Follow‐up on clinical genetics and genomic medicine in Qatar

Author:

Al‐Bader Salha Bujassoum1,Alsulaiman Reem1,Bugrein Hekmet1,Ben Omran Tawfeg234,Abbaszadeh Fatemeh5,Bakheet Nawal1,Apsa Kusasi Sitti1,Abdou Nema1,Solomon Benjamin D.6ORCID,Ghazouani Hafedh1

Affiliation:

1. Department of Medical Oncology, National Center of Cancer Care and Research Hamad Medical Corporation Doha Qatar

2. Section of Clinical and Metabolic Genetics, Department of Pediatrics Hamad Medical Corporation Doha Qatar

3. Weill Cornell Medical College Doha Qatar

4. Sidra Medicine Doha Qatar

5. Diagnostic Molecular Laboratory Hamad Medical Corporation Doha Qatar

6. GeneDx Gaithersburg Maryland

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Reference6 articles.

1. Identifying Lynch Syndrome in Two Families with Classical Hereditary Breast and Ovarian Cancer Syndrome Phenotype: A Case Report

2. Genotype and phenotype correlation of breast cancer in BRCA mutation carriers and noncarriers;Bujassoum S.;Journal of Cancer Science and Therapy,2017

3. Qatar’s experience with hereditary breast and ovarian cancer and high risk clinic: A retrospective study 2013–2016;Bujassoum S.;International Journal of Research,2016

4. Recommendations for follow‐up care of individuals with an inherited predisposition to cancer. II. BRCA1 and BRCA2. Cancer Genetics Studies Consortium;Burke W.;JAMA,1997

5. Recommendations for follow‐up care of individuals with an inherited predisposition to cancer. I. Hereditary nonpolyposis colon cancer. Cancer Genetics Studies Consortium;Burke W.;JAMA,1997

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