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English
Maternal MTR genotype contributes to the risk of non-syndromic cleft lip and palate in the Polish population
scientific article published on 01 June 2006
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
16712703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 January 2020
title
Maternal MTR genotype contributes to the risk of non-syndromic cleft lip and palate in the Polish population
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
16712703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 January 2020
main subject
cleft lip
1 reference
based on heuristic
inferred from title
author
Adrianna Mostowska
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
16712703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 January 2020
Kamil Hozyasz
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
16712703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 January 2020
Paweł Jagodziński
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
16712703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 January 2020
publication date
1 June 2006
1 reference
stated in
Europe PubMed Central
PubMed ID
16712703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 January 2020
published in
Clinical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
16712703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 January 2020
volume
69
1 reference
stated in
Europe PubMed Central
PubMed ID
16712703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 January 2020
issue
6
1 reference
stated in
Europe PubMed Central
PubMed ID
16712703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 January 2020
page(s)
512-517
1 reference
stated in
Europe PubMed Central
PubMed ID
16712703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 January 2020
cites work
Studies of reduced folate carrier 1 (RFC1) A80G and 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms with neural tube and orofacial cleft defects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FJ.1399-0004.2006.00618.X
retrieved
21 January 2018
MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FJ.1399-0004.2006.00618.X
retrieved
21 January 2018
The role of folic acid and Vitamin B12 in genomic stability of human cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FJ.1399-0004.2006.00618.X
retrieved
21 January 2018
Identifiers
DOI
10.1111/J.1399-0004.2006.00618.X
1 reference
stated in
Europe PubMed Central
PubMed ID
16712703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 January 2020
PubMed ID
16712703
1 reference
stated in
Europe PubMed Central
PubMed ID
16712703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 January 2020
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