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English
Low frequency of inherited deletions of 22q11
scientific article published on 01 August 1999
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10405453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10405453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
title
Low frequency of inherited deletions of 22q11
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10405453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10405453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
author name string
A Smith
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10405453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10405453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
L Robson
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10405453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10405453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
publication date
1 August 1999
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10405453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10405453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
published in
American Journal of Medical Genetics Part A
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10405453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10405453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
volume
85
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10405453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10405453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
issue
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10405453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10405453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
page(s)
513-514
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10405453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10405453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
cites work
Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990827%2985%3A5%3C513%3A%3AAID-AJMG16%3E3.0.CO%3B2-J
retrieved
21 January 2018
Nasal dimple as part of the 22q11.2 deletion syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990827%2985%3A5%3C513%3A%3AAID-AJMG16%3E3.0.CO%3B2-J
retrieved
21 January 2018
Idiopathic thrombocytopenic purpura in two mothers of children with DiGeorge sequence: a new component manifestation of deletion 22q11?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990827%2985%3A5%3C513%3A%3AAID-AJMG16%3E3.0.CO%3B2-J
retrieved
21 January 2018
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990827%2985%3A5%3C513%3A%3AAID-AJMG16%3E3.0.CO%3B2-J
retrieved
21 January 2018
Velocardiofacial syndrome and DiGeorge sequence
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990827%2985%3A5%3C513%3A%3AAID-AJMG16%3E3.0.CO%3B2-J
retrieved
21 January 2018
Frequency of inherited deletions of 22q11.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990827%2985%3A5%3C513%3A%3AAID-AJMG16%3E3.0.CO%3B2-J
retrieved
21 January 2018
22q11 deletions in patients with conotruncal heart defects.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990827%2985%3A5%3C513%3A%3AAID-AJMG16%3E3.0.CO%3B2-J
retrieved
21 January 2018
Anal anomalies: an uncommon feature of velocardiofacial (Shprintzen) syndrome?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990827%2985%3A5%3C513%3A%3AAID-AJMG16%3E3.0.CO%3B2-J
retrieved
21 January 2018
Identifiers
DOI
10.1002/(SICI)1096-8628(19990827)85:5<513::AID-AJMG16>3.0.CO;2-J
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10405453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10405453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
PubMed publication ID
10405453
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10405453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10405453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
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