Cite
HARVARD Citation
Harold, D. et al. (2019). Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia. American journal of medical genetics. 180 (3), pp. 223-231. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Harold, D. et al. (2019). Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia. American journal of medical genetics. 180 (3), pp. 223-231. [Online].