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English
Evidence of founder chromosomes in fragile X syndrome
scientific article published on 01 July 1992
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
title
Evidence of founder chromosomes in fragile X syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
main subject
fragile X syndrome
1 reference
based on heuristic
inferred from title
author
Eric J Kremer
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
author name string
Richards RI
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
Holman K
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
Friend K
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
Hillen D
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
Staples A
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
Brown WT
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
Goonewardena P
series ordinal
8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
Tarleton J
series ordinal
9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
Schwartz C
series ordinal
10
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
publication date
1 July 1992
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
volume
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
page(s)
257-260
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng0792-257
0 references
cites work
Fragile X genotype characterized by an unstable region of DNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0792-257
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0792-257
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0792-257
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0792-257
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0792-257
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0792-257
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0792-257
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0792-257
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fragile X families in a northern Swedish county: a genealogical study of possibly affected individuals in the nineteenth century
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0792-257
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0792-257
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0792-257
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning of the essential myotonic dystrophy region and mapping of the putative defect
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0792-257
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary unstable DNA: a new explanation for some old genetic questions?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0792-257
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heritable unstable DNA sequences
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0792-257
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Slippage synthesis of simple sequence DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0792-257
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0792-257
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0792-257
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
PubMed publication ID
1302021
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1302021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
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