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), Cynthia C. Morton(Broad Institute), Jacob A. Reiss, Heather Ferguson(Andrews University), Kate Crow(Kaiser Permanente), Bernd Fritzsch(Nebraska Medical Center), Chantal Kelly(Brigham and Women's Hospital)
Human Genetics
August 25, 2009
Cited by 83


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