Citations for
1BDD, HOXD13
Missense mutations in the homeodomain of HOXD13 are associated with brachydactyly types D and E.
Johnson D, Kan SH, Oldridge M, Trembath RC, Roche P, Esnouf RM, Giele H, Wilkie AO.
Am J Hum Genet 72(4):984-97. Epub 2003 Mar 14. 2003
2BDD
Clinical and molecular studies of brachydactyly type D.
Robin NH, Hurvitz J, Warman ML, Morrison S.
Am J Med Genet 85(4):413-8. 1999