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An n-allele model for progressive amplification in the FMR1 locus

An n-allele model for progressive amplification in the FMR1 locus

http://www.wikidata.org/entity/Q34267174

about

Advances in research on the fragile X syndrome.Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population.Screening for fragile X syndrome: information needs for health planners.The high prevalence of fragile X premutation carrier females: is this frequency unique to the French Canadian population?Single nucleotide polymorphism and FMR1 CGG repeat instability in two Basque valleys.Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: implications for multiple mutational pathways towards fragile X alleles.A survey of FRAXE allele sizes in three populations.

P2860

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P2860

An n-allele model for progressive amplification in the FMR1 locus

http://www.wikidata.org/entity/Q34267174

description

1995 nî lūn-bûn

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1995 թուականի Մայիսին հրատարակուած գիտական յօդուած

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1995 թվականի մայիսին հրատարակված գիտական հոդված

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1995年の論文

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1995年論文

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1995年論文

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1995年論文

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1995年論文

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1995年論文

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1995年论文

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name

An n-allele model for progressive amplification in the FMR1 locus

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An n-allele model for progressive amplification in the FMR1 locus

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An n-allele model for progressive amplification in the FMR1 locus

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type

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An n-allele model for progressive amplification in the FMR1 locus

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An n-allele model for progressive amplification in the FMR1 locus

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An n-allele model for progressive amplification in the FMR1 locus

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prefLabel

An n-allele model for progressive amplification in the FMR1 locus

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An n-allele model for progressive amplification in the FMR1 locus

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An n-allele model for progressive amplification in the FMR1 locus

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Proceedings of the National Academy of Sciences of the United States of America

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An n-allele model for progressive amplification in the FMR1 locus

@en

P2093

Collins A

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Macpherson J

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Morris A

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Nelson D

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Sherman S

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P2860

Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox

Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation

Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general population.

Fragile X syndrome and the (CGG)n mutation: two families with discordant MZ twins.

Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus.

Fragile X syndrome unstable element, p(CCG)n, and other simple tandem repeat sequences are binding sites for specific nuclear proteins.

Reliability of diagnostic assessment of normal and premutation status in the fragile X syndrome using DNA testing.

Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.

Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence.

Population genetics of fragile X: a multiple allele model with variable risk of CGG repeat expansion.

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Newton Ennis Morton

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