Achievements of the European Working Group on Genetics of Hearing Impairment

International Journal of Pediatric Otorhinolaryngology

Volumn 49, Issue SUPPL. 1, 1999, Pages S155-S158

  Martini, A ^a   Mazzoli, M ^a  

^a UNIVERSITY OF FERRARA   (Italy)

Author keywords

Audiology; Congenital deafness; Epidemiology; Genetic disorder; Genetic linkage; Hereditary deafness; Internet

Indexed keywords

AUDIOLOGY; CHILD; CLINICAL PROTOCOL; CONFERENCE PAPER; DATA BASE; FAMILY; GENE MUTATION; GENETIC LINKAGE; GENETICS; HEARING; HEARING IMPAIRMENT; HEARING LOSS; HUMAN; INFANT; NOMENCLATURE; PHENOTYPE; PRACTICE GUIDELINE; PRIORITY JOURNAL;

EID: 0032720158     PISSN: 01655876     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0165-5876(99)00152-4     Document Type: Conference Paper

References (8)

1. W.E. Nance, The genetic analysis of profound prelingual deafness, Birth Defects 16 (1980) 263-269.
2. Hereditary Hearing Loss Homepage: http://dnalab-www.uia.ac.be/dnalab/hhh/
3. Infoletter 1: The HEAR project.
4. Infoletter 2: Audiological and Genetical definitions and protocols - how to collaborate with a genetical laboratory.
5. Infoletter 3: Protocol for cranio-facial malformations associated with hearing loss.
6. Infoletter 4: Internet - The Non-syndromic Hearing Impairment Database and the Hereditary Hearing Loss Homepage.
7. Infoletter 5: Definition of phenotypes.
8. The Non-syndromic Hearing Impairment Database: http:// hear.unife.it/audiology