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English
TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai population.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
17868388
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17868388%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
title
TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai population
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
17868388
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17868388%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
main subject
Thailand
0 references
cleft palate
1 reference
based on heuristic
inferred from title
author
Vorasuk Shotelersuk
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
17868388
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17868388%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
author name string
Suphapeetiporn K
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
17868388
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17868388%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
Tongkobpetch S
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
17868388
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17868388%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
Siriwan P
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
17868388
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17868388%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
publication date
14 September 2007
1 reference
stated in
Europe PubMed Central
PubMed ID
17868388
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17868388%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
published in
Clinical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
17868388
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17868388%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
volume
72
1 reference
stated in
Europe PubMed Central
PubMed ID
17868388
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17868388%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
issue
5
1 reference
stated in
Europe PubMed Central
PubMed ID
17868388
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17868388%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
page(s)
478-483
1 reference
stated in
Europe PubMed Central
PubMed ID
17868388
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17868388%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
Identifiers
DOI
10.1111/J.1399-0004.2007.00891.X
1 reference
stated in
Europe PubMed Central
PubMed ID
17868388
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17868388%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
PubMed ID
17868388
1 reference
stated in
Europe PubMed Central
PubMed ID
17868388
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17868388%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
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