(Q52015413)

19 April 2018

title

Evolutionary dynamics of the FMR1 locus. (English)

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19 April 2018

main subject

Evolutionary dynamics

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2

Morton NE

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19 April 2018

Morris A

1

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19 April 2018

Collins A

series ordinal

3

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19 April 2018

Lawrence S

series ordinal

4

1 reference

19 April 2018

Macpherson JN

series ordinal

5

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19 April 2018

language of work or name

English

0 references

publication date

1 July 1995

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19 April 2018

published in

Annals of Human Genetics

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19 April 2018

volume

59

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19 April 2018

issue

Pt 3

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19 April 2018

page(s)

283-289

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19 April 2018

Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1995.TB00748.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1995.TB00748.X

Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1995.TB00748.X

Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1995.TB00748.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1995.TB00748.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1995.TB00748.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1995.TB00748.X

A complex mutable polymorphism located within the fragile X gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1995.TB00748.X

Fragile X founder chromosome effects: linkage disequilibrium or microsatellite heterogeneity?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1995.TB00748.X

10.1111/J.1469-1809.1995.TB00748.X

21 January 2018

Identifiers

DOI

1 reference

19 April 2018

PubMed ID

7486835

1 reference

19 April 2018