ARTAN, S. Et Al. 2023. A de novo small marker chromosome that causes Trisomy 9p in a patient with failure to develop, microcephaly and normal neuromotor development. 14th European Cytogenomics Conference , (France), 48.

ARTAN, S., ÖZBAKIR, D. H., TOSUMOĞLU, E., HARMANCI, K., PANAL, G., & ERZURUMLUOĞLU GÖKALP, E., (2023). A de novo small marker chromosome that causes Trisomy 9p in a patient with failure to develop, microcephaly and normal neuromotor development . 14th European Cytogenomics Conference (pp.48). , France

ARTAN, SEVİLHAN Et Al. "A de novo small marker chromosome that causes Trisomy 9p in a patient with failure to develop, microcephaly and normal neuromotor development," 14th European Cytogenomics Conference, France, 2023

ARTAN, SEVİLHAN Et Al. "A de novo small marker chromosome that causes Trisomy 9p in a patient with failure to develop, microcephaly and normal neuromotor development." 14th European Cytogenomics Conference , France, pp.48, 2023

ARTAN, S. Et Al. (2023) . "A de novo small marker chromosome that causes Trisomy 9p in a patient with failure to develop, microcephaly and normal neuromotor development." 14th European Cytogenomics Conference , France, p.48.

@conferencepaper{conferencepaper, author={SEVİLHAN ARTAN Et Al. }, title={A de novo small marker chromosome that causes Trisomy 9p in a patient with failure to develop, microcephaly and normal neuromotor development}, congress name={14th European Cytogenomics Conference}, city={}, country={France}, year={2023}, pages={48} }