Associated Papers
Missense mutations in the homeodomain of HOXD13 are associated with brachydactyly types D and E.
Johnson D et al.
American Journal of Human Genetics, 2003
6 Clinical genetics of syn- and brachydactyly: mutations in FGFR2 and HOXD13.
Wilkie A et al.
Journal of Anatomy, 2002
Select a paper to view details