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English
Mutational analysis of mitochondrial DNA of children with Rett syndrome
scientific article published on 01 November 1997
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9436797
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436797%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
title
Mutational analysis of mitochondrial DNA of children with Rett syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9436797
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436797%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
main subject
Rett syndrome
0 references
mutational analysis
1 reference
based on heuristic
inferred from title
author name string
J Tang
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9436797
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436797%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
Y Qi
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9436797
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436797%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
X H Bao
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9436797
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436797%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
X R Wu
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9436797
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436797%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
publication date
1 November 1997
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9436797
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436797%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
published in
Pediatric Neurology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9436797
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436797%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
volume
17
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9436797
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436797%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9436797
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436797%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
page(s)
327-330
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9436797
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436797%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
cites work
Diagnostic criteria for Rett syndrome. The Rett Syndrome Diagnostic Criteria Work Group
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900151-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A simple salting out procedure for extracting DNA from human nucleated cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900151-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of p53 mutations using nonradioactive SSCP analysis: p53 is not frequently mutated in myelodysplastic syndromes (MDS)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900151-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sequence and organization of the human mitochondrial genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900151-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rett syndrome: random X chromosome inactivation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900151-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Current status of genetic research in Rett syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900151-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormal carbohydrate metabolism in cerebrospinal fluid in Rett syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900151-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuropathology of Rett syndrome: case report with neuronal and mitochondrial abnormalities in the brain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900151-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Point mutations in mitochondrial tRNA genes: sequence analysis of chronic progressive external ophthalmoplegia (CPEO)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900151-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900151-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial encephalomyopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900151-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Male Rett variant
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900151-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0887-8994(97)00151-3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9436797
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436797%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
PubMed publication ID
9436797
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9436797
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436797%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
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