(Q58992797)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8162067%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

title

Complex gene conversion events in germline mutation at human minisatellites (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8162067%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8162067%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8162067%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

Jeffreys AJ

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8162067%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

Tamaki K

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8162067%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

MacLeod A

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8162067%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

Neil DL

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8162067%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

language of work or name

English

0 references

publication date

1 February 1994

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8162067%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference

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26 October 2019

volume

1 reference

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26 October 2019

issue

1 reference

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26 October 2019

page(s)

136-145

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8162067%20AND%20SRC:MED&resulttype=core&format=json

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

26 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

Minisatellite repeat coding as a digital approach to DNA typing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

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

https://api.crossref.org/works/10.1038%2FNG0294-136

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

Biology and applications of human minisatellite loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

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%2FNG0294-136

7 January 2021

DNA-minisatellite mutations: recent investigations concerning distribution and impact on parentage testing

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

7 January 2021

Molecular characterization of a spontaneously generated new allele at a VNTR locus: no exchange of flanking DNA sequence

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

7 January 2021

Unequal crossingover between homologous chromosomes is not the major mechanism involved in the generation of new alleles at VNTR loci

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

7 January 2021

Characterization of a panel of highly variable minisatellites cloned from human DNA

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

7 January 2021

Clustering of hypervariable minisatellites in the proterminal regions of human autosomes

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

7 January 2021

Evolutionary transience of hypervariable minisatellites in man and the primates

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

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

https://api.crossref.org/works/10.1038%2FNG0294-136

7 January 2021

Allele-specific MVR-PCR analysis at minisatellite D1S8.

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

7 January 2021

A hypervariable locus D16S309 located at the distal end of 16p.

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

7 January 2021

Minisatellite “isoallele” discrimination in pseudohomozygotes by single molecule PCR and variant repeat mapping

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

7 January 2021

Triplet repeat mutations in human disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

7 January 2021

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%2FNG0294-136

7 January 2021

Gene conversion, recombination nodules, and the initiation of meiotic synapsis

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

7 January 2021

Association of fragile X syndrome with delayed replication of the FMR1 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-136

7 January 2021

Identifiers

DOI

10.1038/NG0294-136

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8162067%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

26 October 2019

1007187153

0 references

Fatcat ID

release_vmxcpahsafh7vgxfr443sqaqk4

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8162067%20AND%20SRC:MED&resulttype=core&format=json