Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
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An Introduction to the Genetics of Normal and Defective HearingMutations of the protocadherin gene PCDH15 cause Usher syndrome type 1FMutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type IIUsher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23USH1A: chronicle of a slow deathUsher syndrome: animal models, retinal function of Usher proteins, and prospects for gene therapyUsher syndrome in the city of Birmingham--prevalence and clinical classificationMyosin VIIA mutation screening in 189 Usher syndrome type 1 patientsMutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse originsGenetic heterogeneity of Usher syndrome type II in a Dutch population.Genetic heterogeneity of Usher syndrome type IIMolecular genetic techniques and applications in ophthalmology.Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreous.Impacts of Usher syndrome type IB mutations on human myosin VIIa motor functionLinkage analysis in Usher syndrome type I (USH1) families from SpainUsher syndrome type III (USH3) linked to chromosome 3q in an Italian family.Evidence for a fourth locus in Usher syndrome type I.Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15.Unconventional myosins and the genetics of hearing loss.Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 gene.Contig maps and genomic sequencing identify candidate genes in the usher 1C locus.Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness.Gene mapping of Usher syndrome type IIa: localization of the gene to a 2.1-cM segment on chromosome 1q41Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate gene ROM1.Analysis of phosducin as a candidate gene for retinopathies.Genetics of chromosome 11: loci for pediatric and adult malignancies, developmental disorders, and other diseases.[Usher syndrome: about a case].Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11.Analysis of two Arab families reveals additional support for a DFNB2 nonsyndromic phenotype of MYO7A.Usher syndrome clinical types I and II: could ocular symptoms and signs differentiate between the two types?From DFNB2 to Usher syndrome: variable expressivity of the same disease.Usher syndrome in the Samaritans: strengths and limitations of using inbred isolated populations to identify genes causing recessive disorders.Usher's syndrome type IC: clinical studies and fine-mapping the disease locus.Ophthalmologic findings in Usher syndrome type 2A.Stable and progressive hearing loss in type 2A Usher's syndrome.Regulation of adenylyl cyclase in LTP
P2860
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P2860
Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
description
1992 nî lūn-bûn
@nan
1992 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
@ast
Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
@en
Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
@nl
type
label
Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
@ast
Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
@en
Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
@nl
prefLabel
Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
@ast
Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
@en
Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
@nl
P2093
P1433
P1476
Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
@en
P2093
C G Möller
I A Priluck
J A Grunkemeyer
J B Kenyon
J Greenberg
M D Weston
P H Beighton
S Davenport
W J Kimberling
P304
P356
10.1016/S0888-7543(05)80121-1
P407
P577
1992-12-01T00:00:00Z