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Clinical Trial Summary

The investigators aim to study the pattern and frequency of pathogenic variants among ALL newly diagnosed cancer patients in a genetically distinct population. Additionally, the investigators will study the uptake rate of "cascade family screening", frequency of pathogenic variants and barriers against testing.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04920513
Study type Observational
Source King Hussein Cancer Center
Contact
Status Active, not recruiting
Phase
Start date May 1, 2021
Completion date December 1, 2024

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