SOĞUKPINAR, M. Et Al. 2023. A Novel ZBTB20 Variant In A Patient With Primrose syndrome: A rare clinical entity. 56th Annual Conference of the European-Society-of-Human-Genetics (ESHG) , (Glasgow, England), 185.

SOĞUKPINAR, M., KARAOSMANOĞLU, B., ÜTİNE, G. E., Boduroglu, K., & Simsek-Kiper, P., (2023). A Novel ZBTB20 Variant In A Patient With Primrose syndrome: A rare clinical entity . 56th Annual Conference of the European-Society-of-Human-Genetics (ESHG) (pp.185). Glasgow, England

SOĞUKPINAR, MERVE Et Al. "A Novel ZBTB20 Variant In A Patient With Primrose syndrome: A rare clinical entity," 56th Annual Conference of the European-Society-of-Human-Genetics (ESHG), Glasgow, England, 2023

SOĞUKPINAR, MERVE Et Al. "A Novel ZBTB20 Variant In A Patient With Primrose syndrome: A rare clinical entity." 56th Annual Conference of the European-Society-of-Human-Genetics (ESHG) , Glasgow, England, pp.185, 2023

SOĞUKPINAR, M. Et Al. (2023) . "A Novel ZBTB20 Variant In A Patient With Primrose syndrome: A rare clinical entity." 56th Annual Conference of the European-Society-of-Human-Genetics (ESHG) , Glasgow, England, p.185.

@conferencepaper{conferencepaper, author={MERVE SOĞUKPINAR Et Al. }, title={A Novel ZBTB20 Variant In A Patient With Primrose syndrome: A rare clinical entity}, congress name={56th Annual Conference of the European-Society-of-Human-Genetics (ESHG)}, city={Glasgow}, country={England}, year={2023}, pages={185} }