Cite
HARVARD Citation
Faivre, L. et al. (2002). Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype. Journal of medical genetics. 39 (8), pp. 594-596. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Faivre, L. et al. (2002). Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype. Journal of medical genetics. 39 (8), pp. 594-596. [Online].