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English
Reply to Amor et al.
scientific article published on 18 January 2012
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355264
retrieved
17 December 2017
reference URL
http://europepmc.org/abstract/PMC/3355264
title
Reply to Amor
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355264
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC3355264&resulttype=core&format=json
retrieved
9 May 2020
author
Nicola Brunetti-Pierri
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355264
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC3355264&resulttype=core&format=json
retrieved
9 May 2020
Pawel Stankiewicz
series ordinal
3
object named as
Paweł Stankiewicz
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355264
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC3355264&resulttype=core&format=json
retrieved
9 May 2020
author name string
Sau Wai Cheung
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355264
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC3355264&resulttype=core&format=json
retrieved
9 May 2020
publication date
18 January 2012
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355264
retrieved
17 December 2017
reference URL
http://europepmc.org/abstract/PMC/3355264
published in
European Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355264
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC3355264&resulttype=core&format=json
retrieved
9 May 2020
volume
20
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355264
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC3355264&resulttype=core&format=json
retrieved
9 May 2020
issue
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355264
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC3355264&resulttype=core&format=json
retrieved
9 May 2020
page(s)
597-597
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355264
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC3355264&resulttype=core&format=json
retrieved
9 May 2020
cites work
Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3355264
retrieved
24 May 2018
4.45 Mb microduplication in chromosome band 14q12 including FOXG1 in a girl with refractory epilepsy and intellectual impairment
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3355264
retrieved
24 May 2018
Atypical Rett syndrome with selective FOXG1 deletion detected by comparative genomic hybridization: case report and review of literature
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3355264
retrieved
24 May 2018
High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3355264
retrieved
24 May 2018
Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screening
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3355264
retrieved
24 May 2018
Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3355264
retrieved
24 May 2018
FOXG1 is responsible for the congenital variant of Rett syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3355264
retrieved
24 May 2018
Winged helix transcription factor BF-1 is essential for the development of the cerebral hemispheres
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3355264
retrieved
24 May 2018
Questionable pathogenicity of FOXG1 duplication.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3355264
retrieved
15 August 2018
West syndrome associated with mosaic duplication ofFOXG1in a patient with maternal uniparental disomy of chromosome 14
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3355264
retrieved
1 December 2018
West syndrome associated with 14q12 duplications harboring FOXG1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FEJHG.2011.270
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Challenges in clinical interpretation of microduplications detected by array CGH analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FEJHG.2011.270
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/EJHG.2011.270
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355264
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC3355264&resulttype=core&format=json
retrieved
9 May 2020
PMC publication ID
3355264
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355264
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC3355264&resulttype=core&format=json
retrieved
9 May 2020
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