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9767506
Source:
http://linkedlifedata.com/resource/pubmed/id/9767506
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47
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Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0030705
,
umls-concept:C1442161
,
umls-concept:C1521101
,
umls-concept:C1853238
pubmed:issue
5
pubmed:dateCreated
1998-11-16
pubmed:abstractText
To ascertain the frequency of 22q11 deletions in a representative population of conotruncal heart defects (CTD) and determine which children are at risk of having a deletion.
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/9005421
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1034-4810
pubmed:author
pubmed-author:BowerCC
,
pubmed-author:HarropKK
,
pubmed-author:LooCC
,
pubmed-author:WalpoleII
,
pubmed-author:WorthingtonSS
pubmed:issnType
Print
pubmed:volume
34
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
438-43
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:9767506-Abnormalities, Multiple
,
pubmed-meshheading:9767506-Adolescent
,
pubmed-meshheading:9767506-Child
,
pubmed-meshheading:9767506-Child, Preschool
,
pubmed-meshheading:9767506-Chromosome Deletion
,
pubmed-meshheading:9767506-Chromosomes, Human, Pair 22
,
pubmed-meshheading:9767506-Craniofacial Abnormalities
,
pubmed-meshheading:9767506-Developmental Disabilities
,
pubmed-meshheading:9767506-Female
,
pubmed-meshheading:9767506-Genetic Testing
,
pubmed-meshheading:9767506-Heart Defects, Congenital
,
pubmed-meshheading:9767506-Humans
,
pubmed-meshheading:9767506-In Situ Hybridization, Fluorescence
,
pubmed-meshheading:9767506-Male
,
pubmed-meshheading:9767506-Pedigree
,
pubmed-meshheading:9767506-Prevalence
,
pubmed-meshheading:9767506-Risk Factors
pubmed:year
1998
pubmed:articleTitle
22q11 deletions in patients with conotruncal heart defects.
pubmed:affiliation
Genetic Services of Western Australia, Princess Margaret Hospital, Subiaco, Western Australia, Australia.
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't