ATİK, T. Et Al. 2022. Identification of the molecular etiology in congenital hemolytic anemias beyond hemoglobinopathies using a targeted next-generation sequencing panel. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1 , 221.

ATİK, T., IŞIK, E., AYDINOK, Y., Orhan, M. F., Oymak, Y., Karakas, Z., ... SARPER, N.(2022). Identification of the molecular etiology in congenital hemolytic anemias beyond hemoglobinopathies using a targeted next-generation sequencing panel. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, 221.

ATİK, TAHİR Et Al. "Identification of the molecular etiology in congenital hemolytic anemias beyond hemoglobinopathies using a targeted next-generation sequencing panel," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, 221, 2022

ATİK, TAHİR Et Al. "Identification of the molecular etiology in congenital hemolytic anemias beyond hemoglobinopathies using a targeted next-generation sequencing panel." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, pp.221, 2022

ATİK, T. Et Al. (2022) . "Identification of the molecular etiology in congenital hemolytic anemias beyond hemoglobinopathies using a targeted next-generation sequencing panel." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, p.221.

@article{article, author={TAHİR ATİK Et Al. }, title={Identification of the molecular etiology in congenital hemolytic anemias beyond hemoglobinopathies using a targeted next-generation sequencing panel}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2022, pages={221} }