Cite
HARVARD Citation
Isojima, T. et al. (n.d.). A recurrent de novo FAM111A mutation causes kenny–caffey syndrome type 2. Journal of bone and mineral research. pp. 992-998. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Isojima, T. et al. (n.d.). A recurrent de novo FAM111A mutation causes kenny–caffey syndrome type 2. Journal of bone and mineral research. pp. 992-998. [Online].