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English
MEF2C haploinsufficiency syndrome: Report of a new MEF2C mutation and review.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
27255693
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27255693%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 April 2020
review article
1 reference
stated in
Europe PubMed Central
title
MEF2C haploinsufficiency syndrome: Report of a new MEF2C mutation and review
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
27255693
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27255693%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 April 2020
main subject
haploinsufficiency
0 references
author
Miguel Leão
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
27255693
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27255693%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 April 2020
author name string
Helena Rocha
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
27255693
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27255693%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 April 2020
Mafalda Sampaio
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
27255693
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27255693%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 April 2020
Ruben Rocha
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
27255693
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27255693%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 April 2020
Susana Fernandes
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
27255693
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27255693%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 April 2020
publication date
31 May 2016
1 reference
stated in
Europe PubMed Central
PubMed ID
27255693
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27255693%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 April 2020
published in
European Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
27255693
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27255693%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 April 2020
volume
59
1 reference
stated in
Europe PubMed Central
PubMed ID
27255693
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27255693%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 April 2020
issue
9
1 reference
stated in
Europe PubMed Central
PubMed ID
27255693
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27255693%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 April 2020
page(s)
478-482
1 reference
stated in
Europe PubMed Central
PubMed ID
27255693
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27255693%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 April 2020
Identifiers
DOI
10.1016/J.EJMG.2016.05.017
1 reference
stated in
Europe PubMed Central
PubMed ID
27255693
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27255693%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 April 2020
PubMed ID
27255693
1 reference
stated in
Europe PubMed Central
PubMed ID
27255693
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27255693%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 April 2020
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