Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28 - Wikidata - wikimedia - TriplyDB

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

http://www.wikidata.org/entity/Q28265989

about

On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP 15) to Xp22.13-p22.11 Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two families Next generation sequencing technology and genomewide data analysis: Perspectives for retinal research Genotype-phenotype correlation in X-linked retinitis pigmentosa 2 (RP2)Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase Linkage analysis of X linked retinitis pigmentosa in the Irish population.Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreous.Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred.A genetic linkage study of a kindred with X-linked retinitis pigmentosa.Molecular genetics of the human X chromosome.A computer programme to calculate risk in X linked disorders using multiple marker loci.Recent advances in the molecular basis of inherited photoreceptor degeneration.Molecular ophthalmology: an update on animal models for retinal degenerations and dystrophies Ocular findings in a form of retinitis pigmentosa with a rhodopsin gene defect.Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27.The golden era of ocular disease gene discovery: race to the finish.Mutations of RPGR in X-linked retinitis pigmentosa (RP3).Retinitis pigmentosa: genes and disease mechanisms.Autosomal dominant retinitis pigmentosa: no evidence for nonallelic genetic heterogeneity on 3q.Linkage heterogeneity between X-linked retinitis pigmentosa and a map of 10 RFLP loci.Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14.Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.Choroideremia is linked to the restriction fragment length polymorphism DXYS1 at XQ13-21.A DNA probe detecting multiple haplotypes of the human Y chromosome.Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis.Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome 1 including the region surrounding the rhesus locus Vision from next generation sequencing: multi-dimensional genome-wide analysis for producing gene regulatory networks underlying retinal development, aging and disease Isolation of polymorphic DNA segments from human chromosome 21.An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 gene.Identifying retinal disease genes: how far have we come, how far do we have to go?Investigation of disease mechanisms in retinitis pigmentosa.Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosa.A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3.

P2860

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P2860

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

http://www.wikidata.org/entity/Q28265989

description

1984 nî lūn-bûn

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1984 թուականի Մայիսին հրատարակուած գիտական յօդուած

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1984 թվականի մայիսին հրատարակված գիտական հոդված

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1984年の論文

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1984年論文

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1984年論文

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1984年論文

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A C Bird

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10.1038/309253A0

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