Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome.
HOXD13 基因突变是 V 型并指和一种新型短指并指综合征的病因
期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1086/511387
Zhao Xiuli, Sun Miao, Zhao Jin, Leyva J Alfonso, Zhu Hongwen, Yang Wei, Zeng Xuan, Ao Yang, Liu Qing, Liu Guoyang, Lo Wilson H Y, Jabs Ethylin Wang, Amzel L Mario, Shan Xiangnian, Zhang Xue
