Browse by Subject MULTIPLE DISLOCATIONS

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Whole-Exome Sequencing Identifies Mutations of KIF22 in Spondyloepimetaphyseal Dysplasia with Joint Laxity, Leptodactylic Type

Min, Byung-Joo; Kim, Namshin; Chung, Taesu; Kim, Ok-Hwa; Nishimura, Gen; Chung, Chin Youb; Song, Hae Ryong; et al, AMERICAN JOURNAL OF HUMAN GENETICS, v.89, no.6, pp.760 - 766, 2011-12

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