GEÇKİNLİ, B. B. Et Al. 2020. Revealing novel splicing mutations in RAB3GAP1 gene causing Warburg Micro syndrome and a case including microduplication of 3q29. ESHG 2020 , (Austria).

GEÇKİNLİ, B. B., TÜRKYILMAZ, A., ALAVANDA, C., TAŞLIDERE, H., SAĞER, S. G., ARSLAN ATEŞ, E., ... SÖYLEMEZ, M. A.(2020). Revealing novel splicing mutations in RAB3GAP1 gene causing Warburg Micro syndrome and a case including microduplication of 3q29 . ESHG 2020, Austria

GEÇKİNLİ, BİLGEN Et Al. "Revealing novel splicing mutations in RAB3GAP1 gene causing Warburg Micro syndrome and a case including microduplication of 3q29," ESHG 2020, Austria, 2020

GEÇKİNLİ, BİLGEN B. Et Al. "Revealing novel splicing mutations in RAB3GAP1 gene causing Warburg Micro syndrome and a case including microduplication of 3q29." ESHG 2020 , Austria, 2020

GEÇKİNLİ, B. B. Et Al. (2020) . "Revealing novel splicing mutations in RAB3GAP1 gene causing Warburg Micro syndrome and a case including microduplication of 3q29." ESHG 2020 , Austria.

@conferencepaper{conferencepaper, author={BİLGEN BİLGE GEÇKİNLİ Et Al. }, title={Revealing novel splicing mutations in RAB3GAP1 gene causing Warburg Micro syndrome and a case including microduplication of 3q29}, congress name={ESHG 2020}, city={}, country={Austria}, year={2020}}