sui karcolás Előjön valamivel ruben genetics of hearing impairment Szeszélyes nap Paplan
Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice | PNAS
Genetics Of Hearing Loss | Aussie Deaf Kids
Resolving the genetic heterogeneity of prelingual hearing loss within one family: Performance comparison and application of two targeted next generation sequencing approaches | Journal of Human Genetics
Clinical characteristics for 100 individuals with apparent genetic deafness | Download Table
Genetic testing as part of the Early Hearing Detection and Intervention (EHDI) process - Genetics in Medicine
Genetics and Age-Related Hearing Loss - ScienceDirect
Diagnostic rates based on clinical characteristics for 100 individuals... | Download Table
Handbook of Genetic Communicative Disorders - 1st Edition
Addressing the Global Neglect of Childhood Hearing Impairment in Developing Countries | PLOS Medicine
JCM | Free Full-Text | Contemporary Speech and Oral Language Care for Deaf and Hard-of-Hearing Children Using Hearing Devices