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Genetic risk factor for unexplained recurrent early pregnancy loss
scientific article published on 01 September 1997
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
9310606
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9310606%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
title
Genetic risk factor for unexplained recurrent early pregnancy loss
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
9310606
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9310606%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
author
Henk J Blom
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
9310606
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9310606%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
Tom Kees Anton Bonifacius Eskes
series ordinal
3
object named as
T K Eskes
1 reference
stated in
Europe PubMed Central
PubMed ID
9310606
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9310606%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
Eric AP Steegers
series ordinal
2
object named as
E A Steegers
1 reference
stated in
Europe PubMed Central
PubMed ID
9310606
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9310606%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
author name string
W L Nelen
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
9310606
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9310606%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
language of work or name
English
0 references
publication date
1 September 1997
1 reference
stated in
Europe PubMed Central
PubMed ID
9310606
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9310606%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
published in
The Lancet
1 reference
stated in
Europe PubMed Central
PubMed ID
9310606
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9310606%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
volume
350
1 reference
stated in
Europe PubMed Central
PubMed ID
9310606
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9310606%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
issue
9081
1 reference
stated in
Europe PubMed Central
PubMed ID
9310606
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9310606%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
page(s)
861
1 reference
stated in
Europe PubMed Central
PubMed ID
9310606
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9310606%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
cites work
Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2924038-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Is the common 677C-->T mutation in the methylenetetrahydrofolate reductase gene a risk factor for neural tube defects? A meta-analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2924038-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Thermolabile methylenetetrahydrofolate reductase in coronary artery disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2924038-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hyperhomocysteinemia: a risk factor in women with unexplained recurrent early pregnancy loss
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2924038-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2924038-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0140-6736(97)24038-9
1 reference
stated in
Europe PubMed Central
PubMed ID
9310606
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9310606%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
PubMed ID
9310606
1 reference
stated in
Europe PubMed Central
PubMed ID
9310606
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9310606%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
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