Guo, Tingwei <br/><br/>
Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients.  [electronic resource] 

 -  Human mutation  Nov 2011 
 - 1278-89 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.21568  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>22q11 Deletion Syndrome--genetics<br/>Cardiovascular Abnormalities--genetics<br/>Chromosomes, Human, Pair 22--genetics<br/>DiGeorge Syndrome--genetics<br/>Genetic Variation<br/>Genotype<br/>Haplotypes<br/>Humans<br/>Phenotype<br/>Polymorphism, Single Nucleotide<br/>T-Box Domain Proteins--genetics