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English
Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: localization to Xq27.3-qter.
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1674730
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1674730%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
title
Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: localization to Xq27.3-qter
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1674730
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1674730%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
author
Ronald Gregg
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1674730
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1674730%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
author name string
A B Metzenberg
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1674730
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1674730%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
K Hogan
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1674730
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1674730%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
G Sekhon
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1674730
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1674730%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
R Laxova
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1674730
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1674730%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
publication date
1 April 1991
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1674730
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1674730%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
published in
Genomics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1674730
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1674730%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
volume
9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1674730
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1674730%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1674730
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1674730%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
page(s)
701-706
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1674730
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1674730%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
Identifiers
DOI
10.1016/0888-7543(91)90363-J
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1674730
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1674730%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
PubMed publication ID
1674730
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1674730
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1674730%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
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