Cite
HARVARD Citation
Dreßen, M. et al. (2016). A novel de novo TBX5 mutation in a patient with Holt–Oram syndrome leading to a dramatically reduced biological function. Molecular genetics & genomic medicine. 4 (5), pp. 557-567. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Dreßen, M. et al. (2016). A novel de novo TBX5 mutation in a patient with Holt–Oram syndrome leading to a dramatically reduced biological function. Molecular genetics & genomic medicine. 4 (5), pp. 557-567. [Online].