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English
Heritable unstable DNA sequences
scientific article published on 01 April 1992
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
1302002
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
title
Heritable unstable DNA sequences
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
1302002
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
main subject
chromosome fragility
1 reference
stated in
Europe PubMed Central
PubMed ID
1302002
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1302002
retrieved
10 September 2022
author name string
Richards RI
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
1302002
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
Sutherland GR
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
1302002
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
language of work or name
English
1 reference
stated in
National Center for Biotechnology Information
PubMed ID
1302002
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1302002
retrieved
10 September 2022
publication date
1 April 1992
1 reference
stated in
Europe PubMed Central
PubMed ID
1302002
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
1302002
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
volume
1
1 reference
stated in
Europe PubMed Central
PubMed ID
1302002
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
page(s)
7-9
1 reference
stated in
Europe PubMed Central
PubMed ID
1302002
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
1302002
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng0492-7
0 references
cites work
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%2FNG0492-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fragile X genotype characterized by an unstable region of DNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0492-7
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%2FNG0492-7
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%2FNG0492-7
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%2FNG0492-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation of sequences that span the fragile X and identification of a fragile X-related CpG island
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0492-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prenatal diagnosis of fragile X syndrome by direct detection of the unstable DNA sequence
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0492-7
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%2FNG0492-7
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%2FNG0492-7
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%2FNG0492-7
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%2FNG0492-7
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%2FNG0492-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0492-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An unstable triplet repeat in a gene related to myotonic muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0492-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0492-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0492-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Absence of expression of the FMR-1 gene in fragile X syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0492-7
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%2FNG0492-7
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%2FNG0492-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Unique organization of the human BCR gene promoter
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0492-7
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%2FNG0492-7
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%2FNG0492-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Positional cloning: let's not call it reverse anymore
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0492-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0492-7
1 reference
stated in
Europe PubMed Central
PubMed ID
1302002
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
PubMed ID
1302002
1 reference
stated in
Europe PubMed Central
PubMed ID
1302002
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1302002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 September 2019
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