Article info
PDFElectronic letters
Assessment of association between variants and haplotypes of the remaining TBX1 gene and manifestations of congenital heart defects in 22q11.2 deletion patients
- Correspondence to: Dr Anita Rauch Institute of Human Genetics, Schwabachanlage 10, 91054 Erlangen, Germany; arauchhumgenet.uni-erlangen.de
Citation
Assessment of association between variants and haplotypes of the remaining TBX1 gene and manifestations of congenital heart defects in 22q11.2 deletion patients
Publication history
- Received June 3, 2003
- Accepted September 5, 2003
- First published April 1, 2004.
Online issue publication
April 27, 2016
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Copyright information
Copyright 2004 Journal of Medical Genetics