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Microdeletion 22q11 and oesophageal atresia
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10051013%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
title
Microdeletion 22q11 and oesophageal atresia
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10051013%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
author name string
Digilio MC
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10051013%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
Marino B
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10051013%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
Bagolan P
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10051013%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
Giannotti A
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10051013%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
Dallapiccola B
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10051013%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
language of work or name
English
0 references
publication date
1 February 1999
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10051013%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10051013%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
volume
36
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10051013%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
issue
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10051013%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
page(s)
137-139
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10051013%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
cites work
Oesophageal atresia: tracheo-oesophageal fistula. A study of survival in 218 infants
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=1734297
retrieved
7 July 2018
Radial aplasia and chromosome 22q11 deletion
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=1734297
retrieved
7 July 2018
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 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=1734297
retrieved
7 July 2018
Chromosome 22q11 microdeletion and isolated conotruncal heart 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=1734297
retrieved
7 July 2018
Anal anomalies: an uncommon feature of velocardiofacial (Shprintzen) 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=1734297
retrieved
7 July 2018
Renal and urological tract malformations caused by a 22q11 deletion
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=1734297
retrieved
7 July 2018
Low-copy-number repeat sequences flank the DiGeorge/velo-cardio-facial syndrome loci at 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=1734297
retrieved
7 July 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=1734297
retrieved
7 July 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=1734297
retrieved
7 July 2018
Esophageal atresia and tracheoesophageal fistula. Review of thirteen years' experience
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=1734297
retrieved
7 July 2018
A population study of the VACTERL association: evidence for its etiologic heterogeneity
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=1734297
retrieved
7 July 2018
Esophageal atresia with distal tracheoesophageal fistula: associated anomalies and prognosis in the 1980s
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=1734297
retrieved
7 July 2018
Oesophageal atresia and associated anomalies
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=1734297
retrieved
7 July 2018
Esophageal atresia and associated anomalies
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=1734297
retrieved
7 July 2018
Esophageal atresia: primary results of 500 consecutively treated patients
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=1734297
retrieved
27 October 2018
Esophageal atresia: five year experience with 148 cases
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=1734297
retrieved
27 October 2018
The VATER association. Analysis of 46 patients
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10051013
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
22q11 deletions in isolated and syndromic patients with tetralogy of Fallot
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10051013
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10051013
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMC publication ID
1734297
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10051013%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
PubMed publication ID
10051013
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734297
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10051013%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
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