Associated Papers
DNA binding analysis of rare variants in homeodomains reveals homeodomain specificity-determining residues.
Kock KH et al.
Nature Communications, 2024
Human HOX gene disorders.
Quinonez SC et al.
Molecular Genetics and Metabolism, 2014
Mutations in the homeodomain of HOXD13 cause syndactyly type 1-c in two Chinese families.
Dai L et al.
Plos One, 2014
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