Hız, A. S. Et Al. 2023. High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases. 55th European Society of Human Genetics Congress , (Vienna, Austria), 466-467.

Hız, A. S., Oktay, Y., Töpf, A., Szabo, N., Güngör, S., Yaramış, A., ... Sönmezler, E.(2023). High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases . 55th European Society of Human Genetics Congress (pp.466-467). Vienna, Austria

Hız, AYŞE Et Al. "High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases," 55th European Society of Human Genetics Congress, Vienna, Austria, 2023

Hız, AYŞE S. Et Al. "High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases." 55th European Society of Human Genetics Congress , Vienna, Austria, pp.466-467, 2023

Hız, A. S. Et Al. (2023) . "High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases." 55th European Society of Human Genetics Congress , Vienna, Austria, pp.466-467.

@conferencepaper{conferencepaper, author={AYŞE SEMRA HIZ Et Al. }, title={High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases}, congress name={55th European Society of Human Genetics Congress}, city={Vienna}, country={Austria}, year={2023}, pages={466-467} }