The molecular and cellular basis of Apert syndrome

来源 :第八届全国医学生物化学与分子生物学、第五届全国临床应用生物化学与分子生物学、2013华东六省一市生物化学与分子生物学联合 | 被引量 : 0次 | 上传用户：xiaogengwhy

【摘要】

：

Apert syndrome(AS) is an autosomal dominant syndrome,characterized by craniosynostosis, midface hypoplasia, and severe syndactyly of the hands and feet, with a prevalence of 1 in 65,000 individuals.

【作者】

：

Liu Chao Cui YaZhou Luan Jing Zhou XiaoYan Han JinXiang

【机构】

：

Shandong Academy of Medical Sciences,Shandong Medical Biotechnology Center,Key Laboratory for Biotec

【出处】

：

第八届全国医学生物化学与分子生物学、第五届全国临床应用生物化学与分子生物学、2013华东六省一市生物化学与分子生物学联合

【发表日期】

：

2013年2期

【关键词】

：

Apert syndrome Fgfr2 Osteoblast pathogenesis

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　　Apert syndrome(AS) is an autosomal dominant syndrome,characterized by craniosynostosis, midface hypoplasia, and severe syndactyly of the hands and feet, with a prevalence of 1 in 65,000 individuals.

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The molecular and cellular basis of Apert syndrome

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