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

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scientific article published on 01 October 1994

Language	Label	Description	Also known as
English	Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism	scientific article published on 01 October 1994

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scholarly article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7842015%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

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

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7842015%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

Darren G Monckton

1

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27 October 2019

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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

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publication date

1 October 1994

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27 October 2019

Nature Genetics

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27 October 2019

8

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27 October 2019

2

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27 October 2019

162-170

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27 October 2019

Minisatellite repeat coding as a digital approach to DNA typing

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-162

21 January 2018

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

1 reference

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21 January 2018

Complex gene conversion events in germline mutation at human minisatellites

1 reference

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21 January 2018

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

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

1 reference

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21 January 2018

Dynamic mutations: a new class of mutations causing human disease

1 reference

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21 January 2018

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

1 reference

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21 January 2018

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

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21 January 2018

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

1 reference

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21 January 2018

A complex mutable polymorphism located within the fragile X gene.

1 reference

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21 January 2018

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

1 reference

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7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-162

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-162

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-162

7 January 2021

based on heuristic

inferred from DOI database lookup

Allele-specific MVR-PCR analysis at minisatellite D1S8.

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-162

7 January 2021

based on heuristic

inferred from DOI database lookup

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

https://api.crossref.org/works/10.1038%2FNG1094-162

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-162

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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7 January 2021

based on heuristic

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

1 reference

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7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-162

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-162

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-162

7 January 2021

based on heuristic

inferred from DOI database lookup

Evidence of founder chromosomes in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-162

7 January 2021

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Striking founder effect for the fragile X syndrome in Finland.

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-162

7 January 2021

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Origin of the expansion mutation in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-162

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-162

7 January 2021

based on heuristic

inferred from DOI database lookup

The sampling theory of selectively neutral alleles

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-162

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-162

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/NG1094-162

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7842015%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7842015%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

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