YILMAZ KARAPINAR, D. Et Al. 2019. Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry. PEDIATRIC BLOOD & CANCER , vol.66, no.10 .

YILMAZ KARAPINAR, D., PATIROĞLU, T., Metin, A., Caliskan, U., Celkan, T., YILMAZ, B., ... Karakas, Z.(2019). Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry. PEDIATRIC BLOOD & CANCER , vol.66, no.10.

YILMAZ KARAPINAR, DENİZ Et Al. "Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry," PEDIATRIC BLOOD & CANCER , vol.66, no.10, 2019

YILMAZ KARAPINAR, DENİZ Y. Et Al. "Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry." PEDIATRIC BLOOD & CANCER , vol.66, no.10, 2019

YILMAZ KARAPINAR, D. Et Al. (2019) . "Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry." PEDIATRIC BLOOD & CANCER , vol.66, no.10.

@article{article, author={DENİZ YILMAZ KARAPINAR Et Al. }, title={Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry}, journal={PEDIATRIC BLOOD & CANCER}, year=2019}