Yılmaz, K. 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 .

Yılmaz, K., Patıroğlu, T., Metın, A., Çalışkan, Ü., Celkan, T. T., Yılmaz, 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.

Yılmaz, Karapınar 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, 2019

Yılmaz, Karapınar 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, 2019

Yılmaz, K. 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.

@article{article, author={Karapınar Yılmaz 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}