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English
Obesity and abnormal behaviour associated with interstitial deletion of chromosome 18 (q12.2q21.1).
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1015541
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2918529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
title
Obesity and abnormal behaviour associated with interstitial deletion of chromosome 18 (q12.2q21.1)
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1015541
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2918529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
author name string
G N Wilson
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1015541
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2918529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
A A Al Saadi
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1015541
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2918529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
language of work or name
English
0 references
publication date
1 January 1989
1 reference
stated in
Europe PubMed Central
PMCID
1015541
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2918529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1015541
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2918529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
volume
26
1 reference
stated in
Europe PubMed Central
PMCID
1015541
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2918529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PMCID
1015541
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2918529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
page(s)
62-63
1 reference
stated in
Europe PubMed Central
PMCID
1015541
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2918529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
cites work
Familial mental retardation in a family with an inherited chromosome rearrangement.
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=1015541
retrieved
14 July 2018
Localization of the gene for familial adenomatous polyposis on chromosome 5.
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=1015541
retrieved
14 July 2018
Syndromes associated with deletion of the long arm of chromosome 18[del(18q)]
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=1015541
retrieved
14 July 2018
Identifiers
DOI
10.1136/JMG.26.1.62
1 reference
stated in
Europe PubMed Central
PMCID
1015541
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2918529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
PMCID
1015541
1 reference
stated in
Europe PubMed Central
PMCID
1015541
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2918529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
PubMed ID
2918529
1 reference
stated in
Europe PubMed Central
PMCID
1015541
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2918529%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
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