SEZER, A. Et Al. 2023. Long-term follow-up and novel variant in Suleiman-El-Hattab syndrome: Expanding the genotypic and clinical spectrum of a rare neurodevelopmental disorder. European Journal of Medical Genetics , vol.66, no.9 .

SEZER, A., KAYHAN, G., & Percin, F. E., (2023). Long-term follow-up and novel variant in Suleiman-El-Hattab syndrome: Expanding the genotypic and clinical spectrum of a rare neurodevelopmental disorder. European Journal of Medical Genetics , vol.66, no.9.

SEZER, ABDULLAH, GÜLSÜM KAYHAN, And Ferda E. Percin. "Long-term follow-up and novel variant in Suleiman-El-Hattab syndrome: Expanding the genotypic and clinical spectrum of a rare neurodevelopmental disorder," European Journal of Medical Genetics , vol.66, no.9, 2023

SEZER, ABDULLAH Et Al. "Long-term follow-up and novel variant in Suleiman-El-Hattab syndrome: Expanding the genotypic and clinical spectrum of a rare neurodevelopmental disorder." European Journal of Medical Genetics , vol.66, no.9, 2023

SEZER, A. KAYHAN, G. And Percin, F. E. (2023) . "Long-term follow-up and novel variant in Suleiman-El-Hattab syndrome: Expanding the genotypic and clinical spectrum of a rare neurodevelopmental disorder." European Journal of Medical Genetics , vol.66, no.9.

@article{article, author={ABDULLAH SEZER Et Al. }, title={Long-term follow-up and novel variant in Suleiman-El-Hattab syndrome: Expanding the genotypic and clinical spectrum of a rare neurodevelopmental disorder}, journal={European Journal of Medical Genetics}, year=2023}