Two families with phenotypically different hereditary low frequency hearing impairment: Longitudinal data and linkage analysis

Scandinavian Audiology

Volumn 30, Issue 4, 2001, Pages 246-254

  Bille, M ^a   Munk Nielsen, L ^a   Tranebjaerg, L ^a   Fagerheim, T ^a   Parving, A ^a  

^a BISPEBJERG HOSPITAL   (Denmark)

Author keywords

Autosomal dominant inheritance; Linkage analysis; Longitudinal data; Low frequency hearing impairment

Indexed keywords

ADULT; ARTICLE; AUDIOLOGY; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 4; FAMILY HISTORY; FEMALE; GENETIC ANALYSIS; GENETIC HETEROGENEITY; GENETIC LINKAGE; HEARING IMPAIRMENT; HUMAN; MAJOR CLINICAL STUDY; MALE; PERCEPTION DEAFNESS; PHENOTYPE; PRIORITY JOURNAL;

ADULT; AUDIOMETRY, PURE-TONE; FEMALE; FOLLOW-UP STUDIES; HEARING LOSS, SENSORINEURAL; HUMANS; LINKAGE (GENETICS); MALE; MIDDLE AGED; PEDIGREE; PHENOTYPE; SEVERITY OF ILLNESS INDEX; SPEECH RECEPTION THRESHOLD TEST;

EID: 0035667080     PISSN: 01050397     EISSN: None     Source Type: Journal    
DOI: 10.1080/01050390152704760     Document Type: Article

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