Browsing by Keyword : Abnormalities, Multiple/*genetics

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Showing results 1 to 2 of 2

Publication YearTitleAJOU
Author
2014Identification of KMT2D and KDM6A mutations by exome sequencing in Korean patients with Kabuki syndrome.손영배정선용
2011Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type.김옥화
1

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