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Issue Date	Title	Journal Title
2013	A novel synonymous mutation causing complete skipping of exon 16 in the SLC26A4 gene in a Korean family with hearing loss	BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
2014	Intrafamilial phenotypic variability in families with biallelic SLC26A4 mutations.	LARYNGOSCOPE
2015	Non-syndromic hearing loss caused by the dominant cis mutation R75Q with the recessive mutation V37I of the GJB2 (Connexin 26) gene	EXPERIMENTAL AND MOLECULAR MEDICINE
1996	Vibrio cholerae non-O1 중이염 1예	Korean Journal of Clinical Pathology(대한임상병리학회지)