Showing results 3 to 5 of 5
Pub Year | Title | AJOU Author(s) | |
---|---|---|---|
2000 | Connexin26 mutations associated with nonsyndromic hearing loss. | 박기현, 박홍준, 전영명, 한시훈 | |
2002 | Functional study of GJB2 in hereditary hearing loss. | 문성균, 정연훈 | |
2012 | PAPSS2 mutations cause autosomal recessive brachyolmia | 김옥화 |