Ergören, M. Et Al. 2019. Application of high-throughput DNA sequencing to score population-specific variants for rare disorders. European Biotechnology Congress , 25.

Ergören, M., Manara, E., Paolucci, S., Temel, S., Mocan, G., DÜNDAR, M., ... Bertelli, M.(2019). Application of high-throughput DNA sequencing to score population-specific variants for rare disorders . European Biotechnology Congress (pp.25).

Ergören, MC Et Al. "Application of high-throughput DNA sequencing to score population-specific variants for rare disorders," European Biotechnology Congress, 2019

Ergören, MC Et Al. "Application of high-throughput DNA sequencing to score population-specific variants for rare disorders." European Biotechnology Congress , pp.25, 2019

Ergören, M. Et Al. (2019) . "Application of high-throughput DNA sequencing to score population-specific variants for rare disorders." European Biotechnology Congress , p.25.

@conferencepaper{conferencepaper, author={MC Ergören Et Al. }, title={Application of high-throughput DNA sequencing to score population-specific variants for rare disorders}, congress name={European Biotechnology Congress}, city={}, country={}, year={2019}, pages={25} }