H. ACER Et Al. , "DIAPH1 homozygous mutation associated with microcephaly, blindness, and seizures," EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France 20- 24 June 2017 , vol.21, pp.60, 2017
ACER, H. Et Al. 2017. DIAPH1 homozygous mutation associated with microcephaly, blindness, and seizures. EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France 20- 24 June 2017 , 60.
ACER, H., CANPOLAT, M., KAYA ÖZÇORA, G. D., & KUMANDAŞ, S., (2017). DIAPH1 homozygous mutation associated with microcephaly, blindness, and seizures . EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France 20- 24 June 2017 (pp.60).
ACER, HAMİT Et Al. "DIAPH1 homozygous mutation associated with microcephaly, blindness, and seizures," EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France 20- 24 June 2017, 2017
ACER, HAMİT Et Al. "DIAPH1 homozygous mutation associated with microcephaly, blindness, and seizures." EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France 20- 24 June 2017 , pp.60, 2017
ACER, H. Et Al. (2017) . "DIAPH1 homozygous mutation associated with microcephaly, blindness, and seizures." EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France 20- 24 June 2017 , p.60.
@conferencepaper{conferencepaper, author={HAMİT ACER Et Al. }, title={DIAPH1 homozygous mutation associated with microcephaly, blindness, and seizures}, congress name={EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France 20- 24 June 2017}, city={}, country={}, year={2017}, pages={60} }