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Nonsyndromic Hereditary Hearing Impairment Pages on BioPortfolio:

BioPortfolio - Nonsyndromic Hereditary Hearing Impairment
Nonsyndromic Hereditary Hearing Impairment - BioPortfolio - Indepth.
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 - 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's Brain and Nervous Diseases Specialized Searches
Nonsyndromic Hereditary Hearing Impairment · Nystagmus Pathologic · Ocular Motility Disorders · Olfactory Nerve · Ophthalmoplegia ...
http://www.bioportfolio.co.uk/web/brain.html...

BioPortfolio - Osmania University - Profile
aminoglycoside-induced non syndromic hearing impairment. Non syndromic hearing impairment is a common sensory disorder, which...28th November, 2009 ...
http://www.bioportfolio.com/biocorporate/7943-Osmania%252525...

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...



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BioPortfolio - GJA3 - gap junction protein, alpha 3, 46kDa
A new large deletion in the DFNB1 locus causes nonsyndromic hearing loss. Mutations in the GJB2 gene encoding the gap junction protein connexin 26. ...
http://www.bioportfolio.com/gene/2700-GJA3.html...

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...

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...

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...

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/...

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...

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/...

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...

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/...

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...

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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