|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
1
|
|
pubmed:dateCreated |
2001-5-7
|
|
pubmed:abstractText |
To clarify the clinical profiles of adolescents and young adults with tetralogy and 22q11.2 deletion, which has recently been identified as a cause of tetralogy of Fallot in about 15% of patients.
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:status |
MEDLINE
|
|
pubmed:issn |
1098-3600
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
3
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
56-60
|
|
pubmed:dateRevised |
2006-11-15
|
|
pubmed:meshHeading |
pubmed-meshheading:11339379-Adolescent,
pubmed-meshheading:11339379-Adult,
pubmed-meshheading:11339379-Age Factors,
pubmed-meshheading:11339379-Chromosome Deletion,
pubmed-meshheading:11339379-Chromosomes, Human, Pair 22,
pubmed-meshheading:11339379-Deafness,
pubmed-meshheading:11339379-Facies,
pubmed-meshheading:11339379-Female,
pubmed-meshheading:11339379-Heart Defects, Congenital,
pubmed-meshheading:11339379-Humans,
pubmed-meshheading:11339379-In Situ Hybridization, Fluorescence,
pubmed-meshheading:11339379-Male,
pubmed-meshheading:11339379-Mental Processes,
pubmed-meshheading:11339379-Psychological Tests,
pubmed-meshheading:11339379-Sex Factors,
pubmed-meshheading:11339379-Tetralogy of Fallot,
pubmed-meshheading:11339379-Time Factors
|
|
pubmed:articleTitle |
Tetralogy of Fallot associated with chromosome 22q11.2 deletion in adolescents and young adults.
|
|
pubmed:affiliation |
Department of Pediatric Cardiology, Tokyo Women's Medical University, Japan.
|
|
pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
|
