R. Holt Et Al. , "Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders," HUMAN GENETICS , vol.136, no.1, pp.119-127, 2017
Holt, R. Et Al. 2017. Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders. HUMAN GENETICS , vol.136, no.1 , 119-127.
Holt, R., Iseri, S. A., Wyatt, A. W., Bax, D. A., Diaz, D. G., Santos, C., ... Broadgate, S.(2017). Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders. HUMAN GENETICS , vol.136, no.1, 119-127.
Holt, R. Et Al. "Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders," HUMAN GENETICS , vol.136, no.1, 119-127, 2017
Holt, R. Et Al. "Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders." HUMAN GENETICS , vol.136, no.1, pp.119-127, 2017
Holt, R. Et Al. (2017) . "Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders." HUMAN GENETICS , vol.136, no.1, pp.119-127.
@article{article, author={R. Holt Et Al. }, title={Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders}, journal={HUMAN GENETICS}, year=2017, pages={119-127} }