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English
CATCH 22.
scientific article published on October 1993
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
editorial
0 references
title
CATCH 22
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
author
Judith Goslin Hall
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
author name string
Hall JG
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016557
retrieved
6 October 2017
language of work or name
English
0 references
publication date
1 October 1993
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
volume
30
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
issue
10
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
page(s)
801-802
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
cites work
DiGeorge syndrome: part of CATCH 22.
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=1016557
retrieved
6 June 2018
Velocardiofacial syndrome in a mother and daughter: variability of the clinical phenotype
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=1016557
retrieved
6 June 2018
Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11
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=1016557
retrieved
6 June 2018
Isolation of a new marker and conserved sequences close to the DiGeorge syndrome marker HP500 (D22S134).
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=1016557
retrieved
6 June 2018
Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis
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=1016557
retrieved
6 June 2018
Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects
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=1016557
retrieved
6 June 2018
Molecular cytogenetics: toward dissection of the contiguous gene syndromes
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=1016557
retrieved
6 June 2018
Contiguous gene syndromes: a component of recognizable syndromes
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=1016557
retrieved
6 June 2018
A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome
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=1016557
retrieved
6 June 2018
Identifiers
DOI
10.1136/JMG.30.10.801
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
PMC publication ID
1016557
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
PubMed publication ID
8230153
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
ResearchGate publication ID
14969441
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