Prelingual Deafness

Known as: Deafness, Prelingual 
 
National Institutes of Health

Papers overview

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2008
2008
CONCLUSION This genetic epidemiological study demonstrated that 26.65% of the prelingual deafness in Northern Chinese patients… (More)
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2007
2007
Neonatal hearing loss is the most frequent sensorial congenital defect in newborns. No data are available on worldwide prevalence… (More)
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Highly Cited
2003
Highly Cited
2003
Purpose: To determine the mutation spectrum of the connexin 26 gene among 324 Taiwanese patients with prelingual deafness and the… (More)
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2002
2002
Mutations in the Cx26 (GJB2) gene have been shown to be responsible for a major part of autosomal recessive non-syndromic… (More)
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2002
2002
OBJECTIVE Mutations in the gene encoding the gap junction protein connexin 26 (GJB2) have been shown as a major contributor to… (More)
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Highly Cited
2002
Highly Cited
2002
BACKGROUND Inherited hearing impairment affects about 1 in 2000 newborns. Up to 50 percent of all patients with autosomal… (More)
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2002
2002
Considerable differences on the frequencies of the mitochondrial 12S rRNA A1555G and tRNASer(UCN) A7445G mutations have been… (More)
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Highly Cited
2000
Highly Cited
2000
Mutations in the connexin 26 gene (GJB2), which encodes a gap-junction protein and is expressed in the inner ear, have been shown… (More)
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Highly Cited
1999
Highly Cited
1999
BACKGROUND DFNB1, the locus of an autosomal recessive form of deafness due to mutations in the connexin-26 gene (CX26 or GJB2) is… (More)
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Highly Cited
1997
Highly Cited
1997
Prelingual non-syndromic (isolated) deafness is the most frequent hereditary sensory defect. In >80% of the cases, the mode of… (More)
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