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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
11857656
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857656%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 May 2020
title
News and comment
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
11857656
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857656%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 May 2020
author
Vicenç Català
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
11857656
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857656%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 May 2020
author name string
Judith Armstrong
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
11857656
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857656%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 May 2020
Pilar Póo
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
11857656
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857656%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 May 2020
Mercè Pineda
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
11857656
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857656%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 May 2020
Elena Aibar
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
11857656
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857656%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 May 2020
Esther Geán
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
11857656
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857656%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 May 2020
Eugènia Monrós
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed ID
11857656
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857656%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 May 2020
publication date
1 November 2001
1 reference
stated in
Europe PubMed Central
PubMed ID
11857656
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857656%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 May 2020
published in
Annals of Neurology
1 reference
stated in
Europe PubMed Central
PubMed ID
11857656
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857656%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 May 2020
volume
50
1 reference
stated in
Europe PubMed Central
PubMed ID
11857656
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857656%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 May 2020
page(s)
696
1 reference
stated in
Europe PubMed Central
PubMed ID
11857656
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857656%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 May 2020
issue
5
1 reference
stated in
Europe PubMed Central
PubMed ID
11857656
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857656%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 May 2020
cites work
Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FANA.1272
retrieved
21 January 2018
Two affected boys in a Rett syndrome family: clinical and molecular findings
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FANA.1272
retrieved
21 January 2018
MECP2 is highly mutated in X-linked mental retardation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FANA.1272
retrieved
21 January 2018
Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FANA.1272
retrieved
21 January 2018
MeCP2 mutations in children with and without the phenotype of Rett syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FANA.1272
retrieved
21 January 2018
Identifiers
DOI
10.1002/ANA.1272
1 reference
stated in
Europe PubMed Central
PubMed ID
11857656
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857656%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 May 2020
PubMed ID
11857656
1 reference
stated in
Europe PubMed Central
PubMed ID
11857656
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857656%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 May 2020
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