Cipe, F. E. Et Al. 2020. A rare case of syndromic severe congenital neutropenia: JAGN1 mutation. TURKISH JOURNAL OF PEDIATRICS , vol.62, no.2 , 326-331.

Cipe, F. E., Aydogmus, C., Baskin, K., KESKİNDEMİRCİ, G., Garncarz, W., & Boztug, K., (2020). A rare case of syndromic severe congenital neutropenia: JAGN1 mutation. TURKISH JOURNAL OF PEDIATRICS , vol.62, no.2, 326-331.

Cipe, Funda Et Al. "A rare case of syndromic severe congenital neutropenia: JAGN1 mutation," TURKISH JOURNAL OF PEDIATRICS , vol.62, no.2, 326-331, 2020

Cipe, Funda E. Et Al. "A rare case of syndromic severe congenital neutropenia: JAGN1 mutation." TURKISH JOURNAL OF PEDIATRICS , vol.62, no.2, pp.326-331, 2020

Cipe, F. E. Et Al. (2020) . "A rare case of syndromic severe congenital neutropenia: JAGN1 mutation." TURKISH JOURNAL OF PEDIATRICS , vol.62, no.2, pp.326-331.

@article{article, author={Funda Erol Cipe Et Al. }, title={A rare case of syndromic severe congenital neutropenia: JAGN1 mutation}, journal={TURKISH JOURNAL OF PEDIATRICS}, year=2020, pages={326-331} }