Identification of a new locus for autosomal dominant non-syndromic hearing impairment (DFNA7) in a large Norwegian family

Human Molecular Genetics

Volumn 5, Issue 8, 1996, Pages 1187-1191

  Fagerheim, T ^a   Nilssen, O ^a   Raeymaekers, P ^b   Brox, V ^a   Moum, T ^a,e   Elverland, H H ^a,f   Teig, E ^c   Omland, H H ^d   Fostad, G K ^d   Tranebjaerg L ^a  

^a UNIVERSITY HOSPITAL OF NORTH NORWAY   (Norway)

^b UNIVERSITY OF LEUVEN   (Belgium)

^c OSLO UNIVERSITY HOSPITAL   (Norway)

^d Levanger Hospital   (Norway)

^e UNIVERSITY OF TROMSØ   (Norway)

^f Østfold Hospital   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

MICROSATELLITE DNA;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 1Q; CLINICAL ARTICLE; FEMALE; GENE LOCUS; GENETIC HETEROGENEITY; GENETIC LINKAGE; HEARING IMPAIRMENT; HUMAN; HUMAN CELL; MALE; NORWAY; PRIORITY JOURNAL;

EID: 10144234815     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.8.1187     Document Type: Article

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