Browsing "Radiology" by Keyword : Craniofacial Abnormalities

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Showing results 1 to 2 of 2

Pub YearTitleAuthor(s)
2011CANT1 mutation is also responsible for Desbuquois dysplasia, type 2 and Kim variant.김옥화
2011Identification of signal peptide domain SOST mutations in autosomal dominant craniodiaphyseal dysplasia.김옥화
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