Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism (Q58992790)

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27 October 2019

title

Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism (English)

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27 October 2019

1

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27 October 2019

author name string

Neumann R

2

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27 October 2019

Guram T

3

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27 October 2019

Fretwell N

4

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27 October 2019

Tamaki K

5

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27 October 2019

MacLeod A

6

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27 October 2019

Jeffreys AJ

7

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27 October 2019

language of work or name

English

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publication date

1 October 1994

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27 October 2019

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27 October 2019

volume

8

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27 October 2019

issue

2

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27 October 2019

page(s)

162-170

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Minisatellite repeat coding as a digital approach to DNA typing

27 October 2019

cites work

1 reference

Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA.

21 January 2018

1 reference

Complex gene conversion events in germline mutation at human minisatellites

21 January 2018

1 reference

A poly(dA.dT) tract is a component of the recombination initiation site at the ARG4 locus in Saccharomyces cerevisiae

21 January 2018

1 reference

A mouse DNA sequence that mediates integration and excision of polyoma virus DNA.

21 January 2018

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Dynamic mutations: a new class of mutations causing human disease

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

A complex mutable polymorphism located within the fragile X gene.

21 January 2018

1 reference

Repeat unit sequence variation in minisatellites: a novel source of DNA polymorphism for studying variation and mutation by single molecule analysis

21 January 2018

1 reference

7 January 2021

Allelic diversity at minisatellite MS205 (D16S309): evidence for polarized variability

1 reference

7 January 2021

Digital DNA typing at a second hypervariable locus by minisatellite variant repeat mapping

1 reference

7 January 2021

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

1 reference

7 January 2021

Tandemly repeated transgenes of the human minisatellite MS32 (D1S8), with novel mouse gamma satellite integration

1 reference

7 January 2021

Allele-specific MVR-PCR analysis at minisatellite D1S8.

1 reference

7 January 2021

Four-state MVR-PCR: increased discrimination of digital DNA typing by simultaneous analysis of two polymorphic sites within minisatellite variant repeats at D1S8.

1 reference

7 January 2021

Sequences flanking the repeat arrays of human minisatellites: association with tandem and dispersed repeat elements.

1 reference

7 January 2021

A family of short, interspersed repeats is associated with tandemly repetitive DNA in the human genome

1 reference

7 January 2021

Identification of a new, abundant superfamily of mammalian LTR-transposons

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7 January 2021

Cloned extrachromosomal circular DNA copies of the human transposable element THE-1 are related predominantly to a single type of family member

1 reference

7 January 2021

A recombination hotspot in the LTR of a mouse retrotransposon identified in an in vitro system

1 reference

7 January 2021

The human THE-LTR(O) and MstII interspersed repeats are subfamilies of a single widely distributed highly variable repeat family

1 reference

7 January 2021

A transposon-like element in the deletion-prone region of the dystrophin gene

1 reference

7 January 2021

Recruitment of multiple alleles within the Eb recombinational hotspot in murine MHC.

1 reference

7 January 2021

Evidence of founder chromosomes in fragile X syndrome

1 reference

7 January 2021

Striking founder effect for the fragile X syndrome in Finland.

1 reference

7 January 2021

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

7 January 2021

Origin of the expansion mutation in myotonic dystrophy

1 reference

7 January 2021

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

1 reference

7 January 2021

The sampling theory of selectively neutral alleles

1 reference

7 January 2021

Minisatellite variant repeat (MVR) mapping: analysis of 'null' repeat units at D1S8

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7 January 2021

Identifiers

DOI

10.1038/NG1094-162

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7842015 AND SRC:MED&resulttype=core&format=json

Dimensions Publication ID

27 October 2019

1013663138

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Fatcat ID

release_5bnynemwgfeqph2ucxdf3oxjmu

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