|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
1
|
|
pubmed:dateCreated |
2008-11-28
|
|
pubmed:abstractText |
22q11.2 Deletion Syndrome (22q11.2DS) is an important genetic syndrome to cardiologists yet remains under-recognized in adults. There is no evidence-based guideline for genetic testing referrals. Feasibility issues in many jurisdictions preclude testing for 22q11.2 deletions in every congenital cardiac patient. We aimed to determine an optimal combination of extracardiac features that could be clinically helpful in identifying adults with tetralogy of Fallot (TOF) and related conotruncal anomalies at highest risk for 22q11.2DS.
|
|
pubmed:grant |
|
|
pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-10334453,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-10509171,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-10842294,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-11280080,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-11339377,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-11392644,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-11803519,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-11835939,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-12639885,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-12765922,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-12892855,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-12902105,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-14681306,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-15509921,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-15708709,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-16208694,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-16418744,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-16547205,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-16641110,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-16730817,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-16824627,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-16908723,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-17210844,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-17391785,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-7677092,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-7688102,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-7759065,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-8230155,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-8522695,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-8660052,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-8677886,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-9350810,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-9708481,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18191243-9737780
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Dec
|
|
pubmed:issn |
1874-1754
|
|
pubmed:author |
|
|
pubmed:issnType |
Electronic
|
|
pubmed:day |
17
|
|
pubmed:volume |
131
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
51-8
|
|
pubmed:dateRevised |
2011-8-1
|
|
pubmed:meshHeading |
pubmed-meshheading:18191243-Adolescent,
pubmed-meshheading:18191243-Adult,
pubmed-meshheading:18191243-Age Factors,
pubmed-meshheading:18191243-Craniofacial Abnormalities,
pubmed-meshheading:18191243-DiGeorge Syndrome,
pubmed-meshheading:18191243-Female,
pubmed-meshheading:18191243-Genetic Testing,
pubmed-meshheading:18191243-Heart Defects, Congenital,
pubmed-meshheading:18191243-Humans,
pubmed-meshheading:18191243-Male,
pubmed-meshheading:18191243-Middle Aged,
pubmed-meshheading:18191243-Predictive Value of Tests,
pubmed-meshheading:18191243-Young Adult
|
|
pubmed:year |
2008
|
|
pubmed:articleTitle |
Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease.
|
|
pubmed:affiliation |
Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
|
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
|
