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-author:ChienPP,
pubmed-author:ClarkB JBJ,
pubmed-author:CuneoB FBF,
pubmed-author:DriscollD ADA,
pubmed-author:EmanuelB SBS,
pubmed-author:FeuerJJ,
pubmed-author:GoldmuntzEE,
pubmed-author:JawadA FAF,
pubmed-author:McDonald-McGinnDD,
pubmed-author:MitchellL ELE,
pubmed-author:ReedLL,
pubmed-author:ZackaiE HEH
|
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.
|