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English
Temple syndrome: improving the recognition of an underdiagnosed chromosome 14 imprinting disorder: an analysis of 51 published cases
scientific article published on 02 June 2014
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24891339
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24891339%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 March 2020
title
Temple syndrome: improving the recognition of an underdiagnosed chromosome 14 imprinting disorder: an analysis of 51 published cases
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24891339
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24891339%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 March 2020
author
Kemi Lokulo-Sodipe
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24891339
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24891339%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 March 2020
Deborah Jg Mackay
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24891339
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24891339%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 March 2020
Justin H Davies
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24891339
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24891339%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 March 2020
Karen Temple
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24891339
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24891339%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 March 2020
author name string
Yiannis Ioannides
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24891339
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24891339%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 March 2020
publication date
2 June 2014
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24891339
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24891339%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 March 2020
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24891339
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24891339%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 March 2020
volume
51
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24891339
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24891339%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 March 2020
issue
8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24891339
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24891339%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 March 2020
page(s)
495-501
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24891339
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24891339%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 March 2020
Identifiers
DOI
10.1136/JMEDGENET-2014-102396
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24891339
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24891339%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 March 2020
PubMed publication ID
24891339
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24891339
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24891339%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 March 2020
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