Cite
HARVARD Citation
Bureau, A. et al. (2019). Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants. Genetic epidemiology. 43 (1), pp. 37-49. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Bureau, A. et al. (2019). Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants. Genetic epidemiology. 43 (1), pp. 37-49. [Online].