SENSORINEURAL HEARING LOSS IN CHILDREN
- 1 December 1996
- journal article
- review article
- Published by Elsevier in Pediatric Clinics of North America
- Vol. 43 (6) , 1195-1216
- https://doi.org/10.1016/s0031-3955(05)70514-9
Abstract
No abstract availableKeywords
This publication has 58 references indexed in Scilit:
- A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locusHuman Molecular Genetics, 1995
- A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3Human Molecular Genetics, 1995
- A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17Nature Genetics, 1995
- A non–syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13qNature Genetics, 1994
- Linkage of usher syndrome type I gene (USH1B) to the long arm of chromosome 11Genomics, 1992
- A gene for usher syndrome type I (USH1A) maps to chromosome 14qGenomics, 1992
- Localization of the gene for branchiootorenal syndrome to chromosome 8qGenomics, 1992
- Clinical variability and genetic heterogeneity within the Acadian Usher populationAmerican Journal of Medical Genetics, 1992
- Isolation of a candidate gene for Norrie disease by positional cloningNature Genetics, 1992
- Sex‐linked recessive congenital deafness and the excess of males in profound childhood deafnessAnnals of Human Genetics, 1965