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Issue Date	Title	Journal Title
2023	Copy-number analysis by base-level normalization: An intuitive visualization tool for evaluating copy number variations	CLINICAL GENETICS
2021	DYNC2H1 variants cause Leber congenital amaurosis without syndromic features	CLINICAL GENETICS
2012	Population-specific spectrum of the F11 mutations in Koreans: evidence for a founder effect.	CLINICAL GENETICS