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Showing results 1 to 3 of 3

Pub YearTitleAJOU Author(s)
2019Deletion of exons 16-17b of CFTR is frequently identified in Korean patients with cystic fibrosis손영배, 장주영
2015Disease-specific growth charts for Korean infants with Prader-Willi syndrome.손영배
2012Molecular genetic analysis of TWIST1 and FGFR3 genes in Korean patients with coronal synostosis: identification of three novel TWIST1 mutations박동하, 윤수한, 정선용
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