Cite
HARVARD Citation
Le Tanno, P. et al. (2017). PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans. Journal of medical genetics. 54 (7), pp. 502-510. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Le Tanno, P. et al. (2017). PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans. Journal of medical genetics. 54 (7), pp. 502-510. [Online].