Nonsyndromic deafness - Genetics Home Reference
Gene Review: Deafness and Hereditary Hearing Loss Overview This link leads ... Isolated deafness; Nonsyndromic hearing impairment; Nonsyndromic hearing loss ...
http://ghr.nlm.nih.gov/condition=nonsyndromicdeafness...
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DFNA25, a Novel Locus for Dominant Nonsyndromic Hereditary Hearing ...
DFNA25, a Novel Locus for Dominant Nonsyndromic Hereditary Hearing Impairment, Maps to 12q21-24. Charles C. Greene,1 Pamella M. McMillan,1 Susan E. Barker,1 ...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1234922/...
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AJHG - DFNA25, a Novel Locus for Dominant Nonsyndromic Hereditary ...
DFNA25, a Novel Locus for Dominant Nonsyndromic Hereditary Hearing Impairment, Maps to 12q21-24. Charles C. Greene1, Pamella M. McMillan1, Susan E. Barker1, ...
http://www.cell.com/AJHG/abstract/S0002-9297(07)62493-8...
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Hereditary Non-Syndromic Sensorineural Hearing Loss
Leaving the patterns of inheritance aside, non-syndromic hearing loss accounts for more than 70% of all hereditary hearing loss. Non-syndromic or isolated ...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1867482/...
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Evidence for digenic inheritance of nonsyndromic hereditary ...
Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family. J Balciuniene, N Dahl, E Borg, E Samuelsson, M J Koisti, ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=13...
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A gene for autosomal dominant nonsyndromic hereditary hearing ...
Mapping genes for nonsyndromic hereditary hearing impairment may lead to identification of genes that are essential for the development and preservation of ...
http://www.ncbi.nlm.nih.gov/pubmed/8595423...
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A new locus for nonsyndromic hereditary hearing impairment, DFNA17 ...
A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=13...
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Nonsyndromic Hearing Loss and Deafness, DFNB1 -- GeneReviews ...
For example, among families segregating autosomal recessive nonsyndromic hearing impairment, GJB2 mutations are causally related to congenital hereditary ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...
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AJHG - Human Nonsyndromic Hereditary Deafness DFNA17 Is Due to a ...
The authors had previously mapped a new locus—DFNA17, for nonsyndromic hereditary hearing impairment—to chromosome 22q12.2-q13.3. DFNA17 spans a 17- to ...
http://www.cell.com/AJHG/abstract/S0002-9297(07)62942-5...
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DFNA2 Nonsyndromic Hearing Loss -- GeneReviews -- NCBI Bookshelf
The diagnosis of DFNA2 nonsyndromic hearing loss should be considered in persons ... (See Deafness and Hereditary Hearing Loss Overview for details about ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...
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