Browsing "Radiology" by Keyword : Mutation, Missense

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Showing results 7 to 8 of 8

Pub YearTitleAuthor(s)
2012TRPV4-pathy manifesting both skeletal dysplasia and peripheral neuropathy: a report of three patients김옥화
2011Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type.김옥화
1

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