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아주대학교 의학문헌정보센터
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Showing results 1 to 3 of 3
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2012
A single recurrent mutation in the 5'-UTR of IFITM5 causes osteogenesis imperfecta type V
김옥화
2010
Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia family.
김옥화
2011
Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type.
김옥화
1
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아주대학교 의학문헌정보센터
