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English
Exclusion mapping of the Cohen syndrome gene from the Prader-Willi syndrome locus
scientific article published on 01 December 1990
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1981180
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1981180%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
title
Exclusion mapping of the Cohen syndrome gene from the Prader-Willi syndrome locus
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1981180
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1981180%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
main subject
Prader–Willi syndrome
1 reference
based on heuristic
inferred from title
Cohen syndrome
1 reference
based on heuristic
inferred from title
Cohen syndrome
1 reference
based on heuristic
inferred from title
author name string
I Kondo
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1981180
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1981180%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
J Hamabe
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1981180
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1981180%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
K Yamamoto
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1981180
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1981180%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
N Niikawa
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1981180
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1981180%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
publication date
1 December 1990
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1981180
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1981180%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
published in
Clinical Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1981180
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1981180%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
volume
38
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1981180
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1981180%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
issue
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1981180
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1981180%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
page(s)
422-426
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1981180
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1981180%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
Identifiers
DOI
10.1111/J.1399-0004.1990.TB03607.X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1981180
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1981180%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
PubMed publication ID
1981180
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1981180
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1981180%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
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