GEÇKİNLİ, B. B. Et Al. 2020. Revealing novel splicing mutations in RAB3GAP1 gene causing Warburg Micro syndrome and a case including microduplication of 3q29. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.SUPPL 1 , 1012-1013.

GEÇKİNLİ, B. B., TÜRKYILMAZ, A., ALAVANDA, C., Taslidere, H., Sager, G., Ates, E. A., ... SÖYLEMEZ, M. A.(2020). Revealing novel splicing mutations in RAB3GAP1 gene causing Warburg Micro syndrome and a case including microduplication of 3q29. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.SUPPL 1, 1012-1013.

GEÇKİNLİ, BİLGEN Et Al. "Revealing novel splicing mutations in RAB3GAP1 gene causing Warburg Micro syndrome and a case including microduplication of 3q29," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.SUPPL 1, 1012-1013, 2020

GEÇKİNLİ, BİLGEN B. Et Al. "Revealing novel splicing mutations in RAB3GAP1 gene causing Warburg Micro syndrome and a case including microduplication of 3q29." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.SUPPL 1, pp.1012-1013, 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." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.SUPPL 1, pp.1012-1013.

@article{article, 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}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2020, pages={1012-1013} }