Introduction to hereditary deafness
Parental narratives on genetic testing for children with hearing loss: A qualitative inquiry
Assessing parental attitudes toward genetic testing for childhood hearing loss: Before and after genetic consultation
A case for genetics education: Collaborating with speech-language pathologists and audiologists
Additional clinical manifestations in children with sensorineural hearing loss and biallelic GJB2 mutations: Who should be offered GJB2 testing?
Compound heterozygosity for dominant and recessive GJB2 mutations: Effect on phenotype and review of the literature
Molecular genetics study of deafness in Brazil: 8-year experience
Molecular study in Brazilian cochlear implant recipients
Genetic epidemiological studies of congenital/prelingual deafness in Turkey: Population structure and mating type are major determinants of mutation identification
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4 : Evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain
A novel splice site mutation in EYA4 causes DFNA10 hearing loss
Identification of novel mutations in WFS1 and genotype–phenotype correlation in Wolfram syndrome
Phenotype description of a Dutch otosclerosis family with suggestive linkage to OTSC7
Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus
Methylthioadenosine phosphorylase ( MTAP ) in hearing: Gene disruption by chromosomal rearrangement in a hearing impaired individual and model organism analysis
Reconnected by sign
Novel syndrome of cataracts, retinitis pigmentosa, late onset deafness and sperm abnormalities: A new Usher syndrome subtype with X-linked inheritance?
Clinical and genetic analysis of two Tunisian otosclerosis families
Familial unilateral deafness and delayed endolymphatic hydrops
Epidemiological study of nonsyndromic hearing loss in Sicilian newborns
Branchio-oto-renal syndrome