Deletion of an enhancer near DLX5 and DLX6 in a family with hearing loss, craniofacial defects, and an inv(7)(q21.3q35)

Kerry K. Brown(Harvard University), Jacob A. Reiss(Kaiser Permanente), Kate Crow(Kaiser Permanente), Heather Ferguson(Brigham and Women's Hospital), Chantal Kelly(Brigham and Women's Hospital), Bernd Fritzsch(University of Iowa), Cynthia C. Morton(Brigham and Women's Hospital)
Human Genetics
August 25, 2009
10.1007/s00439-009-0736-4
Cited by 83Open Access
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