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The study aims to examinethe pattern and frequency of pathogenic variants among all newly diagnosed breast cancer patients in a genetically distinct population. Additionally, the uptake rate of "cascade family screening" , frequency of pathogenic variants and barriers against testing will be studied.
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1,000 participants in 1 patient group
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Hikmat Abdel-Razeq; Rayan Bater
Data sourced from clinicaltrials.gov
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