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English
Facial phenotype allows diagnosis of Mowat-Wilson syndrome in the absence of Hirschsprung disease
scientific article published on 01 January 2004
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
14679597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14679597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 December 2019
title
Facial phenotype allows diagnosis of Mowat-Wilson syndrome in the absence of Hirschsprung disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
14679597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14679597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 December 2019
main subject
Mowat-Wilson syndrome
1 reference
based on heuristic
inferred from title
phenotype
1 reference
based on heuristic
inferred from title
author
Christiane Zweier
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
14679597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14679597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 December 2019
Anita Rauch
series ordinal
4
object named as
Anita Rauch
1 reference
stated in
Europe PubMed Central
PubMed ID
14679597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14679597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 December 2019
Denise Horn
series ordinal
1
object named as
Denise Horn
1 reference
stated in
Europe PubMed Central
PubMed ID
14679597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14679597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 December 2019
author name string
Bernhard Weschke
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
14679597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14679597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 December 2019
publication date
1 January 2004
1 reference
stated in
Europe PubMed Central
PubMed ID
14679597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14679597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 December 2019
published in
American Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
14679597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14679597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 December 2019
volume
124A
1 reference
stated in
Europe PubMed Central
PubMed ID
14679597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14679597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 December 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
14679597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14679597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 December 2019
page(s)
102-104
1 reference
stated in
Europe PubMed Central
PubMed ID
14679597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14679597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 December 2019
Identifiers
DOI
10.1002/AJMG.A.20298
1 reference
stated in
Europe PubMed Central
PubMed ID
14679597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14679597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 December 2019
PubMed ID
14679597
1 reference
stated in
Europe PubMed Central
PubMed ID
14679597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14679597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 December 2019
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