Associated Papers
Recent Advances in Syndactyly: Basis, Current Status and Future Perspectives.
Zaib T et al.
Genes, 2022
Mutations in the homeodomain of HOXD13 cause syndactyly type 1-c in two Chinese families.
Dai L et al.
Plos One, 2014
A splice donor site mutation in HOXD13 underlies synpolydactyly with cortical bone thinning.
Shi X et al.
Gene, 2013
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