Linked Life Data

11850602

Source:http://linkedlifedata.com/resource/pubmed/id/11850602

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2002-2-18
pubmed:abstractText
Microdeletion of 22q11 is responsible for DiGeorge syndrome, velocardiofacial syndrome, congenital conotruncal heart defects, and related disorders. We report our experiences on prenatal diagnosis by fluorescence in situ hybridization (FISH) for 22q11 deletion in two fetuses with tetralogy of Fallot. Karyotyping and FISH of the parents revealed that one fetus inherited the disease from maternal microdeletion. These findings suggest the importance of performing FISH in pregnancies with prenatally detected tetralogy of Fallot.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1011-8934
pubmed:author
pubmed:issnType
Print
pubmed:volume
17
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
125-8
pubmed:dateRevised
2011-3-16
pubmed:meshHeading
pubmed:year
2002
pubmed:articleTitle
Prenatal diagnosis of tetralogy of Fallot associated with chromosome 22q11 deletion.
pubmed:affiliation
Department of Obstetrics, Samsung Cheil Hospital Women's Healthcare Center, Sungkyunkwan University School of Medicine, 1-19 Mookjeung-dong, Choong-gu, Seoul 100-380, Korea.
pubmed:publicationType
Journal Article, Case Reports