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![]() Date: 2011-02-22 05:31:54Nonsyndromic deafness Biology Genetics Sensorineural hearing loss Health GJB2 GJB6 Philosophy of biology Mutation Deafness Mitochondrial diseases Channelopathy | Add to Reading List |
![]() | Microsoft Word - 3 R.S.R.DocID: 17IJX - View Document |
![]() | Gabriel et al. Head & Face Medicine 2012, 8(Suppl 1):O1 http://www.head-face-med.com/content/8/S1/O1 HEAD & FACE MEDICINE ORAL PRESENTATIONDocID: 13m7w - View Document |
![]() | A Novel Homozygous Mutation in the EC1/EC2 Interaction Domain of the Gap Junction Complex Connexon 26 Leads to Profound Hearing ImpairmentDocID: 536t - View Document |
![]() | Visio-hearing loss[removed]edits.vsdDocID: 52q0 - View Document |