Waardenburg's Syndrome Pages on BioPortfolio:

BioPortfolio - Bioportfolio - Gene GB - Disease List
... Autism_Dementia_Ataxia_Loss of Purposeful Hand Use syndrome .... Vrolik disease · Waardenburg syndrome · Warburg Sjo Fledelius Syndrome ...
http://www.bioportfolio.com/gene/disease_list.php...

BioPortfolio.com - BioWeb Mucopolysaccharidosis II Search
HUNTER SYNDROME FACT SHEET Mucopolysaccharidosis Type II (MPS II) What is ... 1 1q USH2 Usher syndrome type II Chromsome 2 2q37 WSI Waardenburg syndrome ...
http://www.bioportfolio.co.uk/cgi-bin/dialogserver.exe?CMD=s...

BioPortfolio.com - BioWeb Plantar Warts Warts Search
... WY - W Syndrome - WA - Waardenburg Syndrome - Waelsch's Syndrome - WAGR Complex .... Pars Planitis - Parsonage Turner Syndrome - Partial 7p Monosomy -. ...
http://www.bioportfolio.co.uk/cgi-bin/dialogserver.exe?CMD=s...

BioPortfolio.com - BioWeb Wegener's Granulomatosis Search
... Waardenburg Syndrome - Waelsch's Syndrome - WAGR Complex - WAGR Syndrome .... Arthritis Sjoegren's Syndrome Behcet's Syndrome Relapsing Polychondritis ...
http://www.bioportfolio.co.uk/cgi-bin/dialogserver.exe?CMD=s...

BioPortfolio "Fraser syndrome 1" Antibody
Waardenburg syndrome in man and splotch mutants in the mouse: a paradigm of the usefulness of linkage and synteny homologies in mouse and man for the ...
http://www.bioportfolio.co.uk/antibody/Fraser%20syndrome%201...

BioPortfolio Syndrome Antibody
The mutation of Mi causes Waardenburg Syndrome type II in humans. Source:Recombinant human MiTF protein encoding aa 170-279 expressed in E.coli ...
http://www.bioportfolio.co.uk/antibody/anti-Syndrome.htm...

BioPortfoliocom BioWeb Auditory Tumor Acoustic Neuroma Search
... syndrome type II Chromsome 2 2q37 WSI Waardenburg syndrome type I 19350 Chromosome 4 4q12 PBT Piebald trait* 17280 4q23 q27 RGS Rieger syndrome* 18050 ...
http://www.bioportfolio.co.uk/cgi-bin/dialogserver.exe?CMD=s...

BioPortfoliocom BioWeb Nonsyndromic Hereditary Hearing Impairment ...
Bloom Syndrome Canavan Disease Cystic Fibrosis Familial Dysautonomia Fanconi ... of Hearing Impairment Consortium conference on Waardenburg syndrome s ...
http://www.bioportfolio.co.uk/cgi-bin/dialogserver.exe?CMD=s...

Results from other life science and pharmaceutical sites:

Waardenburg's Syndrome
Waardenburg's Syndrome is a rare disorder that results from an autosomal dominant mutation as a deletion in Pax-3. Some of the characteristics of this ...
http://www.brown.edu/Courses/BI0032/neurcrst/waar.htm...

Waardenburg syndrome - Genetics Home Reference
Waardenburg syndrome is a group of genetic conditions that can cause hearing loss and changes in coloring (pigmentation) of the hair, skin, and eyes. ...
http://ghr.nlm.nih.gov/condition=waardenburgsyndrome...

Waardenburg Syndrome Type I -- GeneReviews -- NCBI Bookshelf
Waardenburg syndrome type I (WS1) is an auditory-pigmentary disorder comprising congenital sensorineural hearing loss and pigmentary disturbances of the ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...

Waardenburg Syndrome [NIDCD Health Information]
Waardenburg syndrome (WS) is an inherited disorder often characterized by ... Other individuals with Waardenburg syndrome may have unusually brilliant blue ...
http://www.nidcd.nih.gov/health/hearing/waard.asp...

Waardenburg Syndrome Type 1
15 May 2006 ... Waardenburg syndrome (WS) is a rare disease characterized by sensorineural ... Otopathology in a case of type I Waardenburg's syndrome. ...
http://www.medscape.com/viewarticle/531762...

Heterogeneity in Waardenburg syndrome.
Heterogeneity of Waardenburg syndrome is demonstrated in a review of 1285 patients from the literature and 34 previously unreported patients in five ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=16...

Epistatic relationship between Waardenburg Syndrome genes MITF and ...
Waardenburg syndrome (WS) is a hereditary disorder that causes hypopigmentation and hearing impairment. Depending on additional symptoms, WS is classified ...
http://www.nature.com/ng/journal/v18/n3/abs/ng0398-283.html...

Homozygosity for Waardenburg syndrome.
Baldwin CT, Hoth CF, Amos JA, da-Silva EO, Milunsky A. An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome. Nature. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=18...

Waardenburg's syndrome patients have mutations in the human ...
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene. Mayada Tassabehji*, Andrew P. Read*†, Valerie E. Newton‡ ...
http://www.nature.com/nature/journal/v355/n6361/abs/355635a0...

Neurological phenotype in Waardenburg syndrome type 4 correlates ...
Waardenburg syndrome type 4 (WS4), also called Shah-Waardenburg syndrome, is a rare neurocristopathy that results from the absence of melanocytes and ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=13...

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