Yılmaz Karapınar, 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 and Cancer , vol.66, no.10 .

Yılmaz Karapınar, D., Patıroğlu, T., Metin, A., Çalışkan, Ü., Celkan, T., YILMAZ, B., ... Karakaş, 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 and Cancer , vol.66, no.10.

Yılmaz Karapınar, Deniz 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 and Cancer , vol.66, no.10, 2019

Yılmaz Karapınar, Deniz 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 and Cancer , vol.66, no.10, 2019

Yılmaz Karapınar, 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 and Cancer , vol.66, no.10.

@article{article, author={Deniz Yılmaz Karapınar 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 and Cancer}, year=2019}