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Publications by Denise Yan
Novel Missense Mutations in MYO7A Underlying Postlingual High- Or Low-Frequency Non-Syndromic Hearing Impairment in Two Large Families From China
Journal of Human Genetics
Genetics
Screening of Deafness-Causing DNA Variants That Are Common in Patients of European Ancestry Using a Microarray-Based Approach
PLoS ONE
Multidisciplinary
Novel Mutations Confirm That COL11A2 Is Responsible for Autosomal Recessive Non-Syndromic Hearing Loss DFNB53
Molecular Genetics and Genomics
Medicine
Genetics
Molecular Biology
Absence of GJB2 Gene Mutations, the GJB6 Deletion (GJB6-D13S1830) and Four Common Mitochondrial Mutations in Nonsyndromic Genetic Hearing Loss in a South African Population
International Journal of Pediatric Otorhinolaryngology
Medicine
Otorhinolaryngology
Pediatrics
Perinatology
Child Health
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