A novel MSX1 intronic mutation associated with autosomal dominant non-syndromic oligodontia in a large Chinese family pedigree

Autor: Xue, Jinjie, Gao, Qingping, Huang, Yanru, Zhang, Xiaoyu, Yang, Pu, Cram, David S., Liang, Desheng, Wu, Lingqian
Zdroj: In Clinica Chimica Acta 1 October 2016 461:135-140
Databáze: ScienceDirect
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