KADER, Ş. Et Al. 2018. Homozygous congenital factor VII deficiency with a novel mutation, associated with severe spontaneous intracranial bleeding in a neonate. BLOOD COAGULATION & FIBRINOLYSIS , vol.29, no.5 , 476-480.

KADER, Ş., MUTLU, M., Acar, F. A., ASLAN, Y., & BAHADIR, A., (2018). Homozygous congenital factor VII deficiency with a novel mutation, associated with severe spontaneous intracranial bleeding in a neonate. BLOOD COAGULATION & FIBRINOLYSIS , vol.29, no.5, 476-480.

KADER, ŞEBNEM Et Al. "Homozygous congenital factor VII deficiency with a novel mutation, associated with severe spontaneous intracranial bleeding in a neonate," BLOOD COAGULATION & FIBRINOLYSIS , vol.29, no.5, 476-480, 2018

KADER, ŞEBNEM Et Al. "Homozygous congenital factor VII deficiency with a novel mutation, associated with severe spontaneous intracranial bleeding in a neonate." BLOOD COAGULATION & FIBRINOLYSIS , vol.29, no.5, pp.476-480, 2018

KADER, Ş. Et Al. (2018) . "Homozygous congenital factor VII deficiency with a novel mutation, associated with severe spontaneous intracranial bleeding in a neonate." BLOOD COAGULATION & FIBRINOLYSIS , vol.29, no.5, pp.476-480.

@article{article, author={ŞEBNEM KADER Et Al. }, title={Homozygous congenital factor VII deficiency with a novel mutation, associated with severe spontaneous intracranial bleeding in a neonate}, journal={BLOOD COAGULATION & FIBRINOLYSIS}, year=2018, pages={476-480} }