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Nonsyndromic Hereditary Hearing Impairment Pages on BioPortfolio:
Results from other life science and pharmaceutical sites:
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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Nonsyndromic hereditary hearing loss.
Nonsyndromic hereditary hearing loss. Li XC, Friedman RA. Section on Hereditary Diseases of the Ear, Department of Cell and Molecular Biology, ...
http://www.ncbi.nlm.nih.gov/pubmed/12391618...
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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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Evidence for digenic inheritance of nonsyndromic hereditary ...
Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish fami...Evidence for digenic inheritance of nonsyndromic hereditary ...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1377400/...
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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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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.ncbi.nlm.nih.gov/pmc/articles/PMC1377736/...
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AJHG - Evidence for Digenic Inheritance of Nonsyndromic Hereditary ...
Evidence for Digenic Inheritance of Nonsyndromic Hereditary Hearing Loss in a Swedish Family. Jorune Balciuniene1, Niklas Dahl2, Erik Borg3, Eva Samuelsson4 ...
http://www.cell.com/AJHG/abstract/S0002-9297(07)61380-9...
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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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PAS-01-036: GENETIC TESTING AND THE CLINICAL MANAGEMENT OF ...
GENETIC TESTING AND THE CLINICAL MANAGEMENT OF NONSYNDROMIC HEREDITARY HEARING IMPAIRMENT Release Date: December 20, 2000 PA NUMBER: PAS-01-036 National ...
http://grants.nih.gov/grants/guide/pa-files/PAS-01-036.html...
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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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