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Genetic variation and evolutionary stability of the FMR1 CGG repeat in six closed human populations
scientific article published on 01 July 1996
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
8826480
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8826480%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
title
Genetic variation and evolutionary stability of the FMR1 CGG repeat in six closed human populations
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
8826480
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8826480%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
main subject
human population genetics
1 reference
based on heuristic
inferred from title
genetic variation
1 reference
based on heuristic
inferred from title
author name string
Eichler EE
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
8826480
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8826480%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
Nelson DL
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
8826480
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8826480%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
publication date
1 July 1996
1 reference
stated in
Europe PubMed Central
PubMed ID
8826480
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8826480%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
published in
American Journal of Medical Genetics Part A
1 reference
stated in
Europe PubMed Central
PubMed ID
8826480
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8826480%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
volume
64
1 reference
stated in
Europe PubMed Central
PubMed ID
8826480
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8826480%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
page(s)
220-225
1 reference
stated in
Europe PubMed Central
PubMed ID
8826480
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8826480%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
8826480
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8826480%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
cites work
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
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reference URL
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High resolution of human evolutionary trees with polymorphic microsatellites
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Fragile X founder effect?
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Absence of polymorphism at the ZFY locus on the human Y chromosome
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Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups
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21 January 2018
Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions.
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21 January 2018
Length of uninterrupted CGG repeats determines instability in the FMR1 gene
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Crossref
reference URL
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21 January 2018
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
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21 January 2018
Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland
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21 January 2018
Precursor arrays for triplet repeat expansion at the fragile X locus
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21 January 2018
Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs
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21 January 2018
Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.
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21 January 2018
Construction of a GT polymorphism map of human 9q
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21 January 2018
An n-allele model for progressive amplification in the FMR1 locus
1 reference
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21 January 2018
Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus
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Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome
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21 January 2018
Absence of expression of the FMR-1 gene in fragile X syndrome
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21 January 2018
Frequency and stability of the fragile X premutation.
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Fragile-X syndrome in Hawaii: a summary of clinical experience
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Evidence of founder chromosomes in fragile X syndrome
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Human genes containing polymorphic trinucleotide repeats
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Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation
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PCR amplification and analysis of yeast artificial chromosomes
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Preventive screening for the fragile X syndrome
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Population screening for fragile X
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Population incidence and segregation ratios in the Martin-Bell syndrome.
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Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms
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A second-generation linkage map of the human genome
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21 January 2018
Fragile X genotype characterized by an unstable region of DNA.
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21 January 2018
A complex mutable polymorphism located within the fragile X gene.
1 reference
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retrieved
21 January 2018
Identifiers
DOI
10.1002/(SICI)1096-8628(19960712)64:1<220::AID-AJMG40>3.0.CO;2-M
0 references
PubMed ID
8826480
1 reference
stated in
Europe PubMed Central
PubMed ID
8826480
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8826480%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
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