Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1998-9-1
pubmed:abstractText
This study was designed to determine the frequency of 22q11 deletions in a large, prospectively ascertained sample of patients with conotruncal defects and to evaluate the deletion frequency when additional cardiac findings are also considered.
pubmed:grant
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0735-1097
pubmed:author
pubmed:issnType
Print
pubmed:volume
32
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
492-8
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:9708481-Aorta, Thoracic, pubmed-meshheading:9708481-Child, pubmed-meshheading:9708481-Chromosome Deletion, pubmed-meshheading:9708481-Chromosomes, Human, Pair 22, pubmed-meshheading:9708481-DiGeorge Syndrome, pubmed-meshheading:9708481-Double Outlet Right Ventricle, pubmed-meshheading:9708481-Face, pubmed-meshheading:9708481-Female, pubmed-meshheading:9708481-Genetic Testing, pubmed-meshheading:9708481-Heart Defects, Congenital, pubmed-meshheading:9708481-Heart Septal Defects, Ventricular, pubmed-meshheading:9708481-Humans, pubmed-meshheading:9708481-Incidence, pubmed-meshheading:9708481-Male, pubmed-meshheading:9708481-Prospective Studies, pubmed-meshheading:9708481-Pulmonary Artery, pubmed-meshheading:9708481-Syndrome, pubmed-meshheading:9708481-Tetralogy of Fallot, pubmed-meshheading:9708481-Transposition of Great Vessels, pubmed-meshheading:9708481-Truncus Arteriosus, Persistent
pubmed:year
1998
pubmed:articleTitle
Frequency of 22q11 deletions in patients with conotruncal defects.
pubmed:affiliation
The Children's Hospital of Philadelphia, Department of Pediatrics, University of Pennsylvania Medical Center, 19104, USA. goldmuntz@email.chop.edu
pubmed:publicationType
Journal Article, Comparative Study, Research Support, U.S. Gov't, P.H.S.