Cite
APA Citation
Rauch, A., Devriendt, K., Koch, A., Rauch, R., Gewillig, M., Kraus, C., Weyand, M., Singer, H., Reis, A., & Hofbeck, M. (2004). assessment of association between variants and haplotypes of the remaining TBX1 gene and manifestations of congenital heart defects in 22q11.2 deletion patients. Journal of medical genetics, 41(4), e40. http://access.bl.uk/ark:/81055/vdc_100135178858.0x000048