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DiGeorge syndrome: part of CATCH 22.
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scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016569
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230162%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
title
DiGeorge syndrome: part of CATCH 22
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016569
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230162%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
main subject
DiGeorge syndrome
1 reference
based on heuristic
inferred from title
author
John Burn
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016569
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230162%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
Peter J Scambler
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016569
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230162%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
Judith A Goodship
series ordinal
4
object named as
J Goodship
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016569
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230162%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
author name string
D I Wilson
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016569
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230162%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
language of work or name
English
0 references
publication date
1 October 1993
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016569
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230162%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
1016569
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230162%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
volume
30
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016569
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230162%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
issue
10
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016569
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230162%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
page(s)
852-856
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016569
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230162%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
cites work
Noonan's and DiGeorge syndromes with monosomy 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=1016569
retrieved
21 June 2018
The velo-cardio-facial syndrome: a clinical and genetic analysis
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=1016569
retrieved
21 June 2018
Microdeletions within 22q11 associated with sporadic and familial DiGeorge 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=1016569
retrieved
21 June 2018
DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin
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=1016569
retrieved
21 June 2018
Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge 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=1016569
retrieved
21 June 2018
Deletions and microdeletions of 22q11.2 in 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=1016569
retrieved
21 June 2018
A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 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=1016569
retrieved
21 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=1016569
retrieved
21 June 2018
Truncus arteriosus and facial dysmorphism
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=1016569
retrieved
30 October 2018
Systemic treatment of early breast cancer by hormonal, cytotoxic, or immune therapy. 133 randomised trials involving 31,000 recurrences and 24,000 deaths among 75,000 women. Early Breast Cancer Trialists' Collaborative Group
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8230162
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Deletions within chromosome 22q11 in familial congenital heart disease
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8230162
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A deletion in chromosome 22 can cause DiGeorge syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8230162
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Spectrum of Di George syndrome in patients with truncus arteriosus: Expanded Di George syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8230162
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.30.10.852
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016569
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230162%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
PMC publication ID
1016569
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016569
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230162%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
PubMed publication ID
8230162
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016569
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8230162%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
ResearchGate publication ID
14969450
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