Title: Clinical utility gene card for: DiGeorge syndrome, velocardiofacial syndrome, Shprintzen syndrome, chromosome 22q11.2 deletion syndrome (22q11.2, TBX1)
Authors: Schwinger, Eberhard ×
Devriendt, Koenraad
Rauch, Anita
Philip, Nicole #
Issue Date: Sep-2010
Publisher: Karger
Series Title: European Journal of Human Genetics vol:18 issue:9
Article number: 10.1038/ejhg.2010.5.
ISSN: 1018-4813
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Department of Human Genetics - miscellaneous
× corresponding author
# (joint) last author

Files in This Item:
File Description Status SizeFormat
SchwingerE-pub.pdfpublisher's version pdf Published 153KbAdobe PDFView/Open Request a copy

These files are only available to some KU Leuven Association staff members


All items in Lirias are protected by copyright, with all rights reserved.

© Web of science