Evidence of founder chromosomes in fragile X syndrome (Q67482177)

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13 September 2019

title

Evidence of founder chromosomes in fragile X syndrome (English)

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13 September 2019

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13 September 2019

Richards RI

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13 September 2019

Holman K

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13 September 2019

Friend K

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13 September 2019

Hillen D

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13 September 2019

Staples A

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13 September 2019

Brown WT

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13 September 2019

Goonewardena P

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13 September 2019

Tarleton J

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13 September 2019

Schwartz C

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13 September 2019

publication date

1 July 1992

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13 September 2019

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13 September 2019

volume

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13 September 2019

issue

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13 September 2019

page(s)

257-260

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Fragile X genotype characterized by an unstable region of DNA.

13 September 2019

cites work

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https://api.crossref.org/works/10.1038%2FNG0792-257

7 January 2021

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-257

7 January 2021

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-257

7 January 2021

Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-257

7 January 2021

Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-257

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-257

7 January 2021

Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-257

7 January 2021

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-257

7 January 2021

Fragile X families in a northern Swedish county: a genealogical study of possibly affected individuals in the nineteenth century

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-257

7 January 2021

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-257

7 January 2021

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-257

7 January 2021

Cloning of the essential myotonic dystrophy region and mapping of the putative defect

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-257

7 January 2021

Hereditary unstable DNA: a new explanation for some old genetic questions?

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-257

7 January 2021

Heritable unstable DNA sequences

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-257

7 January 2021

Slippage synthesis of simple sequence DNA

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-257

7 January 2021

The use of synthetic tandem repeats to isolate new VNTR loci: cloning of a human hypermutable sequence

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-257

7 January 2021

Identifiers

DOI

10.1038/NG0792-257

1 reference

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13 September 2019

1 reference

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