Cite
HARVARD Citation
Pinz, H. et al. (2018). De novo variants in Myelin regulatory factor (MYRF) as candidates of a new syndrome of cardiac and urogenital anomalies. American journal of medical genetics. 176 (4), pp. 969-972. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Pinz, H. et al. (2018). De novo variants in Myelin regulatory factor (MYRF) as candidates of a new syndrome of cardiac and urogenital anomalies. American journal of medical genetics. 176 (4), pp. 969-972. [Online].