(Q35881955)

English

Mutation rate in the hypervariable VNTR g3 (D7S22) is affected by allele length and a flanking DNA sequence polymorphism near the repeat array

scientific article published in August 1996

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Mutation rate in the hypervariable VNTR g3 (D7S22) is affected by allele length and a flanking DNA sequence polymorphism near the repeat array (English)

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

author name string

Andreassen R

1

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Egeland T

2

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Olaisen B

3

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

language of work or name

0 references

publication date

1 August 1996

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

59

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

2

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

360-367

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914730

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914730

11 July 2018

Complex recombination events at the hypermutable minisatellite CEB1 (D2S90).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914730

11 July 2018

Length of uninterrupted CGG repeats determines instability in the FMR1 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914730

11 July 2018

cDNA clones contain autonomous replication activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914730

11 July 2018

Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914730

11 July 2018

Structure of the 5' ends of immunoglobulin genes: a novel conserved sequence

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914730

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914730

11 July 2018

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914730

11 July 2018

Slipped-strand mispairing: a major mechanism for DNA sequence evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914730

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914730

11 July 2018

Cloning a selected fragment from a human DNA 'fingerprint': isolation of an extremely polymorphic minisatellite

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914730

11 July 2018

Minisatellite repeat coding as a digital approach to DNA typing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914730

11 July 2018

Chemiluminescent DNA probes: evaluation and usefulness in forensic cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914730

11 July 2018

Highly polymorphic minisatellite sequences: allele frequencies and mutation rates for five locus-specific probes in a Caucasian population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914730

24 September 2018

OBP100 binds remarkably degenerate octamer motifs through specific interactions with flanking sequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/8755922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8755922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of a European collaborative exercise comparing DNA typing results using a single locus VNTR probe

1 reference

https://pubmed.ncbi.nlm.nih.gov/8755922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for point mutations by semi-automated DNA sequencing using sequenase and magnetic beads

1 reference

https://pubmed.ncbi.nlm.nih.gov/8755922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human VNTR mutation and sex

1 reference

https://pubmed.ncbi.nlm.nih.gov/8755922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8755922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complex gene conversion events in germline mutation at human minisatellites

1 reference

https://pubmed.ncbi.nlm.nih.gov/8755922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/8755922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous mutation in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/8755922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correct transcription of an immunoglobulin κ gene requires an upstream fragment containing conserved sequence elements

1 reference

https://pubmed.ncbi.nlm.nih.gov/8755922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

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