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Non-syndromic, autosomal-recessive deafness.
Clin Genet. 2006 May;69(5):371-92. doi: 10.1111/j.1399-0004.2006.00613.x.
Clin Genet. 2006.
PMID: 16650073
Review.
The wide range of functions of these DFNB genes reflects the heterogeneity of the genes involved in hearing and hearing loss. Several of these genes are involved in both recessive and dominant deafness, or in both non-syndromic and syndromic deafness. …
The wide range of functions of these DFNB genes reflects the heterogeneity of the genes involved in hearing and hearing los …
Features of autosomal recessive non-syndromic hearing impairment: a review to serve as a reference.
Oonk AM, Huygen PL, Kunst HP, Kremer H, Pennings RJ.
Oonk AM, et al.
Clin Otolaryngol. 2016 Oct;41(5):487-97. doi: 10.1111/coa.12567. Epub 2016 Feb 11.
Clin Otolaryngol. 2016.
PMID: 26474130
Review.
OBJECTIVE: Non-syndromic sensorineural hearing impairment is inherited in an autosomal recessive fashion in 75-85% of cases. ...CONCLUSION: This review aims to serve as a summary and a reference for counselling purposes when a causative gene has been i …
OBJECTIVE: Non-syndromic sensorineural hearing impairment is inherited in an autosomal recessive fashion in 75-85 …
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[Genetics of congenital deafness].
Faundes V, Pardo RA, Castillo Taucher S.
Faundes V, et al.
Med Clin (Barc). 2012 Oct 20;139(10):446-51. doi: 10.1016/j.medcli.2012.02.014. Epub 2012 Apr 24.
Med Clin (Barc). 2012.
PMID: 22538062
Review.
Spanish.
Congenital deafness is defined as the hearing loss which is present at birth and, consequently, before speech development. ...More than 400 syndromes accompanied of deafness have been described, which represent about 30% of cases of congenital hearing loss …
Congenital deafness is defined as the hearing loss which is present at birth and, consequently, before speech development. ... …
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