Clinical utility gene card for: DiGeorge syndrome, velocardiofacial syndrome, Shprintzen syndrome, chromosome 22q11.2 deletion syndrome (22q11.2, TBX1).

Authors :: Schwinger E
Devriendt K
Rauch A
Philip N
Source :: European journal of human genetics : EJHG [Eur J Hum Genet] 2010 Sep; Vol. 18 (9). Date of Electronic Publication: 2010 Feb 03.
Publication Year :: 2010

Subjects :: DiGeorge Syndrome diagnosis
Humans
Sensitivity and Specificity
Chromosome Deletion
Chromosomes, Human, Pair 22
DiGeorge Syndrome genetics

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