KAYGUSUZ, E. 2022. De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway (Davetli Konuşmacı). 8th International Congress of the Molecular Biology Association of Turkey , (İstanbul, Turkey).

KAYGUSUZ, E., (2022). De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway (Davetli Konuşmacı) . 8th International Congress of the Molecular Biology Association of Turkey, İstanbul, Turkey

KAYGUSUZ, EMRAH. "De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway (Davetli Konuşmacı)," 8th International Congress of the Molecular Biology Association of Turkey, İstanbul, Turkey, 2022

KAYGUSUZ, EMRAH. "De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway (Davetli Konuşmacı)." 8th International Congress of the Molecular Biology Association of Turkey , İstanbul, Turkey, 2022

KAYGUSUZ, E. (2022) . "De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway (Davetli Konuşmacı)." 8th International Congress of the Molecular Biology Association of Turkey , İstanbul, Turkey.

@conferencepaper{conferencepaper, author={EMRAH KAYGUSUZ}, title={De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway (Davetli Konuşmacı)}, congress name={8th International Congress of the Molecular Biology Association of Turkey}, city={İstanbul}, country={Turkey}, year={2022}}