Ognenovski, M. Et Al. 2016. Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease. Arthritis and Rheumatology , vol.68, no.5 , 1272-1280.

Ognenovski, M., Renauer, P., Gensterblum, E., Kotter, I., Xenitidis, T., Henes, J. C., ... Casali, B.(2016). Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease. Arthritis and Rheumatology , vol.68, no.5, 1272-1280.

Ognenovski, Mikhail Et Al. "Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease," Arthritis and Rheumatology , vol.68, no.5, 1272-1280, 2016

Ognenovski, Mikhail Et Al. "Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease." Arthritis and Rheumatology , vol.68, no.5, pp.1272-1280, 2016

Ognenovski, M. Et Al. (2016) . "Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease." Arthritis and Rheumatology , vol.68, no.5, pp.1272-1280.

@article{article, author={Mikhail Ognenovski Et Al. }, title={Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease}, journal={Arthritis and Rheumatology}, year=2016, pages={1272-1280} }