Nonsyndromic Hereditary Hearing Impairment Pages on BioPortfolio:

BioPortfolio's Brain and Nervous Diseases News Feed
Nonsyndromic Hereditary Hearing Impairment · Nystagmus Pathologic · Ocular Motility Disorders · Olfactory Nerve · Ophthalmoplegia ...
http://www.bioportfolio.co.uk/news/brain.html...

BioPortfolio - Nonsyndromic Hereditary Hearing Impairment - InDepth
Nonsyndromic hereditary hearing impairment (NSHHI) is a highly...4th May, 2005 ... A new locus for nonsyndromic hereditary hearing impairment, DFNA17, ...
http://www.bioportfolio.com/indepth/Nonsyndromic_Hereditary_...

BioPortfolio's Ear, Nose and Throat Conditions News Feed
Nonsyndromic Hereditary Hearing Impairment · Nose Neoplasms · Oropharyngeal Neoplasms · Otitis Media Ear Infections · Otitis Media Effusion ...
http://www.bioportfolio.co.uk/news/ear.html...

BioPortfolio - Vestibular Aqueduct - InDepth
Rapid umbilical cord diagnostic of hereditary profound hearing loss: how we do it. ... analysis of nonsyndromic hearing impairment from typical areas in ...
http://www.bioportfolio.com/indepth/Vestibular_Aqueduct.pdf...

BioPortfolio's Rare Diseases News Feed
Nonsyndromic Hereditary Hearing Impairment · Nose Neoplasms · Obsessive- Compulsive Disorder · Ochronosis · Oculodentodigital · Oligodendroglioma ...
http://www.bioportfolio.co.uk/news/rare.shtml...

BioPortfolio - Bioportfolio - Gene GB - Disease List
... Autosomal recessive nonsyndromic hearing loss · Autosomal Recessive Sensorineural Hearing Impairment and Goiter · AxD · Ayerza syndrome ...
Hereditary arthro_ophthalmopathy · Hereditary coproporphyria · Hereditary
dystopic lipidosis ...
http://www.bioportfolio.com/gene/disease_list.php...

BioPortfolio - Bioportfolio - Gene GB - Disease List
... recessive form of juvenile ALS type 3 · Autosomal recessive nonsyndromic hearing loss · Autosomal Recessive Sensorineural Hearing Impairment and Goiter
...
http://www.bioportfolio.com/antibody/disease_list.php...

Biotechnology, Pharmaceutical and Life Science Email addresses for ...
BioPortfolio the comprehensive email list supplier for data, information, search engine and services on biotechnology, pharmaceutical and healthcare ...
http://www.bioportfolio.com/advertis/bioemail.htm...

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...

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/...

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...

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...

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...

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...

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...

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...

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...

Human Nonsyndromic Hereditary Deafness DFNA17 Is Due to a Mutation ...
The authors had previously mapped a new locus—DFNA17, for nonsyndromic hereditary hearing impairment—to chromosome 22q12.2-q13.3. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=12...

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