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DEAFNESS, CHILDHOOD-ONSET NEUROSENSORY, AUTOSOMAL RECESSIVE 8

Known as: NSRD8, Neurosensory Nonsyndromic Recessive Deafness 8, DEAFNESS, AUTOSOMAL RECESSIVE 8 
 
National Institutes of Health

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Highly Cited
2012
Highly Cited
2012
PURPOSE The aim of the present study was to evaluate the potential morphologic risk factors for postoperative neurosensory… Expand
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Highly Cited
2011
Highly Cited
2011
BACKGROUND: Many preterm children display school difficulties, which may be mediated by impairment in executive function and… Expand
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Highly Cited
2010
Highly Cited
2010
PURPOSE To elucidate the relationship between the anatomic position of the inferior alveolar nerve (IAN) at the mandibular second… Expand
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2003
2003
Congenital hearing loss occurs in approximately 1 in 1000 live births and 60% of these cases are hereditary.1,2 Non-syndromic… Expand
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Highly Cited
2002
Highly Cited
2002
PURPOSE This study evaluated the location of the mandibular canal in the ramus of the mandible before bilateral sagittal split… Expand
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Highly Cited
2001
Highly Cited
2001
Approximately 50% of childhood deafness is caused by mutations in specific genes. Autosomal recessive loci account for… Expand
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Highly Cited
2001
Highly Cited
2001
Editor—Congenital deafness occurs in approximately 1 in 1000 live births and 50% of these cases are hereditary. Non-syndromic… Expand
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Highly Cited
2001
Highly Cited
2001
Abstract. Two loci for nonsyndromic recessive deafness located on chromosome 21q22.3 have previously been reported, DFNB8 and… Expand
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Highly Cited
1997
Highly Cited
1997
This retrospective study evaluated neurosensory dysfunction and the implant success rate associated with 64 implants placed in 15… Expand
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Highly Cited
1994
Highly Cited
1994
PURPOSE This article addresses the suitability of semirigid fixation for the treatment of mandibular fractures. MATERIALS AND… Expand
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