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English
Empirical recurrence risk after unidentified multiple congenital abnormalities.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6644767%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 October 2019
title
Empirical recurrence risk after unidentified multiple congenital abnormalities
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6644767%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 October 2019
author name string
A Czeizel
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6644767%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 October 2019
J Métneki
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6644767%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 October 2019
language of work or name
English
0 references
publication date
1 October 1983
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6644767%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 October 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6644767%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 October 2019
volume
20
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6644767%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 October 2019
issue
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6644767%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 October 2019
page(s)
367-371
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6644767%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 October 2019
cites work
Multiple congenital dislocations associated with characteristic facial abnormality
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049152
retrieved
21 June 2018
Evaluation of information-guidance genetic counselling
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049152
retrieved
21 June 2018
[Contribution to the study of the heredity of epibulbar dermoids]
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6644767
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The syndrome of goldenhar affecting two siblings
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6644767
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Schisis-association
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6644767
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Definition of multiple congenital abnormalities
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6644767
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Increased frequency of neural tube defects in sibs of children with other malformations
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6644767
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Spectrum of anomalies in the Meckel syndrome, or: "Maybe there is a malformation syndrome with at least one constant anomaly"
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6644767
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.20.5.367
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6644767%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 October 2019
PMC publication ID
1049152
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6644767%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 October 2019
PubMed publication ID
6644767
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049152
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6644767%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 October 2019
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