Pages that link to "Q30487513"

The following pages link to Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss (Q30487513):

Displaying 9 items.

• A Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic Family (Q28116585) (← links)
• Demographically-Based Evaluation of Genomic Regions under Selection in Domestic Dogs (Q28273884) (← links)
• Massively Parallel Sequencing for Genetic Diagnosis of Hearing Loss: The New Standard of Care (Q38267074) (← links)
• Exome sequencing and whole genome sequencing for the detection of copy number variation (Q38531649) (← links)
• Short Report - Clinical Genetics Genomic copy number alterations in non-syndromic hearing loss (Q50351695) (← links)
• Overlapping 16p13.11 deletion and gain of copies variations associated with childhood onset psychosis include genes with mechanistic implications for autism associated pathways: Two case reports. (Q52884385) (← links)
• The ancient sarcomeric myosins found in specialized muscles (Q64065699) (← links)
• Expression of Normally Repressed Myosin Heavy Chain 7b in the Mammalian Heart Induces Dilated Cardiomyopathy (Q92305570) (← links)
• Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF (Q92392997) (← links)