Sezer, A. Et Al. 2020. An infant with two de novo variants causing recessive and dominant disorders: Diagnostic challenge. 53rd European Society of Human Genetics (ESHG) , (Berlin, Germany), 98-99.

Sezer, A., Gündoğdu Öğütlü, Ö. B., Türkyılmaz, Z., Gücüyener, K., Kayhan, G., & Perçin, F. E., (2020). An infant with two de novo variants causing recessive and dominant disorders: Diagnostic challenge . 53rd European Society of Human Genetics (ESHG) (pp.98-99). Berlin, Germany

Sezer, Abdullah Et Al. "An infant with two de novo variants causing recessive and dominant disorders: Diagnostic challenge," 53rd European Society of Human Genetics (ESHG), Berlin, Germany, 2020

Sezer, Abdullah Et Al. "An infant with two de novo variants causing recessive and dominant disorders: Diagnostic challenge." 53rd European Society of Human Genetics (ESHG) , Berlin, Germany, pp.98-99, 2020

Sezer, A. Et Al. (2020) . "An infant with two de novo variants causing recessive and dominant disorders: Diagnostic challenge." 53rd European Society of Human Genetics (ESHG) , Berlin, Germany, pp.98-99.

@conferencepaper{conferencepaper, author={Abdullah Sezer Et Al. }, title={An infant with two de novo variants causing recessive and dominant disorders: Diagnostic challenge}, congress name={53rd European Society of Human Genetics (ESHG)}, city={Berlin}, country={Germany}, year={2020}, pages={98-99} }