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

✍ Scribed by Schwinger, Eberhard; Devriendt, Koen; Rauch, Anita; Philip, Nicole

Book ID: 109849395
Publisher: Nature Publishing Group
Year: 2010
Tongue: English
Weight: 149 KB
Volume: 18
Category: Article
ISSN: 1018-4813
DOI: 10.1038/ejhg.2010.5

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