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Clinical Phenotype and CARD15 Gene Mutation with Blau Syndrome in Chinese Children and Their Parents
[会议论文] 作者：Cai-feng Li,Xiao-hu He,Jun-mei Zhang,Tong-xin Han,Wei-ying Kuang,
来源：第五届亚洲儿科研究大会 年份：2009
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Analysis of clinical manifestations and treatment in 26 children with fibrodysplasia ossificans prog
[期刊论文] 作者：Jun-Mei Zhang,Cai-Feng Li,Shuang-Ying Ke,Yu-Rong Piao,Tong-Xin Han,Wei-Ying Kuang,Jiang Wang,iang-Hong,
来源：世界儿科杂志（英文版） 年份：2020
Background Fibrodysplasia ossificans progressiva (FOP) is a rare and disabling heritable connective tissue disease that is difficult to treat.This study seeks t...
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