Associated Papers
Missense variants of FBN2 associated with congenital arachnodactyly in three Chinese families.
Sui Y et al.
Molecular Genetics and Metabolism Reports, 2024
Whole exome sequencing identifies a novel missense FBN2 mutation co-segregating in a four-generation Chinese family with congenital contractural arachnodactyly.
Guo X et al.
Bmc Medical Genetics, 2016
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