Mutation screening of the EXT1 and EXT2 genes in patients with hereditary multiple exostoses.

Hereditary multiple exostoses (HME), the most frequent of all skeletal dysplasias, is an autosomal dominant disorder characterized by the presence of multiple exostoses localized mainly at the end of long bones. HME is genetically heterogeneous, with at least three loci, on 8q24.1 (EXT1), 11p11-p13...

詳細記述

書誌詳細
主要な著者: Philippe, C, Porter, D, Emerton, M, Wells, D, Simpson, A, Monaco, A
フォーマット: Journal article
言語:English
出版事項: 1997