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

Eberhard Schwinger*, Koen Devriendt, Anita Rauch, Nicole Philip

*Corresponding author for this work
8 Citations (Scopus)
Original languageEnglish
JournalEuropean Journal of Human Genetics
Issue number9
Number of pages1
Publication statusPublished - 01.09.2010
Externally publishedYes

Research Areas and Centers

  • Research Area: Medical Genetics

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