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Division Of Genetic Disease National Institute Of Health | 論文

• Association study of semaphorin 7a (sema7a) polymorphisms with bone mineral density and fracture risk in postmenopausal Korean women
• The molecular basis of phenylketonuria in Koreans
• Characterization of 458 single nucleotide polymorphisms of disease candidate genes in the Korean population
• Identification and functional analysis of cystathionine beta-synthase gene mutations in patients with homocystinuria
• The Molecular Basis of Phenylketonuria in Koreans
• Identification of cartilage oligomeric matrix protein (COMP) gene mutations in patients with pseudoachondroplasia and multiple epiphyseal dysplasia
• Prevalence of congenital malformations and genetic diseases in Korea

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