Browsing by Author "Kenna, Margaret"

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High-Throughput Detection of Mutations Responsible for Childhood Hearing Loss Using Resequencing Microarrays

Kothiyal, Prachi; Cox, Stephanie; Ebert, Jonathan; Husami, Ammar; Kenna, Margaret Alene; Greinwald, John H.; Aronow, Bruce J.; Rehm, Heidi L. (BioMed Central, 2010)

Background: Despite current knowledge of mutations in 45 genes that can cause nonsyndromic sensorineural hearing loss (SNHL), no unified clinical test has been developed that can comprehensively detect mutations in multiple ...