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FMR1 triplet arrays: paying the price for perfection
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
8558550
retrieved
28 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
FMR1 triplet arrays: paying the price for perfection
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
8558550
retrieved
28 July 2017
author name string
Hirst MC
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
8558550
retrieved
28 July 2017
language of work or name
English
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publication date
1 October 1995
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stated in
Europe PubMed Central
PubMed ID
8558550
retrieved
28 July 2017
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
8558550
retrieved
28 July 2017
volume
32
1 reference
stated in
Europe PubMed Central
PubMed ID
8558550
retrieved
28 July 2017
page(s)
761-763
1 reference
stated in
Europe PubMed Central
PubMed ID
8558550
retrieved
28 July 2017
issue
10
1 reference
stated in
Europe PubMed Central
PubMed ID
8558550
retrieved
28 July 2017
cites work
Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051695
retrieved
21 June 2018
Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051695
retrieved
21 June 2018
Frequency and stability of the fragile X premutation.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051695
retrieved
21 June 2018
Length of uninterrupted CGG repeats determines instability in the FMR1 gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051695
retrieved
21 June 2018
Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051695
retrieved
21 June 2018
Unusual (CGG)n expansion and recombination in a family with fragile X and DiGeorge syndrome
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051695
retrieved
21 June 2018
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051695
retrieved
21 June 2018
Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus
1 reference
stated in
PubMed Central
reference URL
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retrieved
21 June 2018
Apparent regression of the CGG repeat in FMR1 to an allele of normal size.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051695
retrieved
30 October 2018
Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051695
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30 October 2018
Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051695
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30 October 2018
Somatic mosaicism in sperm is associated with intergenerational (CAG)n changes in Huntington disease.
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30 October 2018
A novel repeat structure at the myotonic dystrophy locus in a 37 repeat allele with unexpectedly high stability
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051695
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30 October 2018
Haplotype analysis at the FRAXA locus in the Japanese population
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8558550
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Precursor arrays for triplet repeat expansion at the fragile X locus
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8558550
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
CAG repeat length variation in sperm from a patient with Kennedy's disease
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8558550
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.32.10.761
1 reference
stated in
Europe PubMed Central
PubMed ID
8558550
retrieved
28 July 2017
PMCID
1051695
1 reference
stated in
Europe PubMed Central
PubMed ID
8558550
retrieved
28 July 2017
PubMed ID
8558550
1 reference
stated in
Europe PubMed Central
PubMed ID
8558550
retrieved
28 July 2017
ResearchGate publication ID
14641076
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