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Eur J Hum Genet. 2010 Sep;18(9). doi: 10.1038/ejhg.2010.5. Epub 2010 Feb 3.

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

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1
Institute of Human Genetics, University Hospital Schleswig-Holstein, L├╝beck, Germany. schwing@uni-luebeck.de
PMID:
20125192
PMCID:
PMC2987430
DOI:
10.1038/ejhg.2010.5
[Indexed for MEDLINE]
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