A novel intragenic microdeletion in RUNX2 in a Chinese family with cleidocranial
在锁骨颅骨发育不全的中国家系中发现一个新的RUNX2基因内微片断缺失，张婷婷，孙迎春，目的：锁骨颅骨发育不全（CCD）是一种罕见的常染色体显性遗传性骨骼发育不良性疾病，以颅骨、锁骨，和牙齿异常为主要特征。目前认
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