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Whole exome sequencing identifies a novel missense FBN2 mutation co-segregating in a four-generation Chinese family with congenital contractural arachnodactyly
Shanxi Population and Family Planning Research Institute, Shanxi Key Laboratory of Birth Defects and Cell Regeneration, Taiyuan, People’s Republic of China
Shanxi Population and Family Planning Research Institute, Shanxi Key Laboratory of Birth Defects and Cell Regeneration, Taiyuan, People’s Republic of China
Shanxi Population and Family Planning Research Institute, Shanxi Key Laboratory of Birth Defects and Cell Regeneration, Taiyuan, People’s Republic of China
Shanxi Population and Family Planning Research Institute, Shanxi Key Laboratory of Birth Defects and Cell Regeneration, Taiyuan, People’s Republic of China
Shanxi Population and Family Planning Research Institute, Shanxi Key Laboratory of Birth Defects and Cell Regeneration, Taiyuan, People’s Republic of China
Shanxi Population and Family Planning Research Institute, Shanxi Key Laboratory of Birth Defects and Cell Regeneration, Taiyuan, People’s Republic of China
Shanxi Population and Family Planning Research Institute, Shanxi Key Laboratory of Birth Defects and Cell Regeneration, Taiyuan, People’s Republic of China
Shanxi Population and Family Planning Research Institute, Shanxi Key Laboratory of Birth Defects and Cell Regeneration, Taiyuan, People’s Republic of China
Shanxi Population and Family Planning Research Institute, Shanxi Key Laboratory of Birth Defects and Cell Regeneration, Taiyuan, People’s Republic of China
Shanxi Population and Family Planning Research Institute, Shanxi Key Laboratory of Birth Defects and Cell Regeneration, Taiyuan, People’s Republic of China