Population-based genetic study of childhood hearing impairment in the Trent Region of the United Kingdom.

Parker, M J; Fortnum, H M; Young, I D; Davis, A C; Mueller, R F

Parker, M J; Fortnum, H M; Young, I D; Davis, A C; Mueller, R F.

Affiliation

Parker MJ; MRC Institute of Hearing Research, University Park, Nottingham, United Kingdom.

Audiology ; 39(4): 226-31, 2000.

Article in En | MEDLINE | ID: mdl-10963445

Subject(s)

Hearing Disorders/genetics; Population Surveillance; Adolescent; Catchment Area, Health; Child; Child, Preschool; Connexin 26; Connexins/genetics; DNA Mutational Analysis; Female; Genetic Counseling; Hearing Disorders/diagnosis; Humans; Male; Point Mutation/genetics; Severity of Illness Index; Surveys and Questionnaires; United Kingdom/epidemiology

Search on Google

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Population Surveillance / Hearing Disorders Type of study: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Country/Region as subject: Europa Language: En Journal: Audiology Year: 2000 Document type: Article

Search on Google

XML

PubMed Links