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English
EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) is on 7p11.2-q21.3
scientific article published on 01 August 1992
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1424230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1424230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
title
EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) is on 7p11.2-q21.3
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1424230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1424230
retrieved
25 September 2022
main subject
ectodermal dysplasia
1 reference
based on heuristic
inferred from title
ectrodactyly
1 reference
based on heuristic
inferred from title
ectrodactyly–ectodermal dysplasia–cleft syndrome
1 reference
based on heuristic
inferred from title
chromosome abnormality
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1424230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1424230
retrieved
25 September 2022
author
Mazin Qumsiyeh
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1424230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1424230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
language of work or name
English
1 reference
stated in
National Center for Biotechnology Information
PubMed publication ID
1424230
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1424230
retrieved
25 September 2022
publication date
1 August 1992
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1424230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1424230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
published in
Clinical Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1424230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1424230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
volume
42
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1424230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1424230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1424230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1424230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
page(s)
101
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1424230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1424230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
Identifiers
DOI
10.1111/J.1399-0004.1992.TB03149.X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1424230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1424230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
PubMed publication ID
1424230
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1424230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1424230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
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