Min, B., Kim, N., Chung, T., Kim, O., Nishimura, G., Chung, C., . . . Cho, T. (2011). Whole-Exome Sequencing Identifies Mutations of KIF22 in Spondyloepimetaphyseal Dysplasia with Joint Laxity, Leptodactylic Type. Elsevier.
Stile di citazione ChicagoMin, Byung-Joo, et al. Whole-Exome Sequencing Identifies Mutations of KIF22 in Spondyloepimetaphyseal Dysplasia With Joint Laxity, Leptodactylic Type. Elsevier, 2011.
Citazione MLAMin, Byung-Joo, et al. Whole-Exome Sequencing Identifies Mutations of KIF22 in Spondyloepimetaphyseal Dysplasia With Joint Laxity, Leptodactylic Type. Elsevier, 2011.
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