5 results on '"Karaca, Ender"'
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2. The impact of the Turkish population variome on the genomic architecture of rare disease traits
3. DLG2 intragenic exonic deletions reinforce the link to neurodevelopmental disorders and suggest a potential association with congenital anomalies and dysmorphism
4. The impact of the Turkish (TK) population variome on the genomic architecture of rare disease traits
5. P691: Elevating pharmacogenomics: A tailored in-house solution for empowering accurate clinical decision support
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