C. S. Kasapkara Et Al. , "When a common symptom of a neonate become an unusual diagnosis: A case report of HMG-CoA lyase deficiency with a novel mutation," Gazi Medical Journal , vol.30, no.3, pp.298-299, 2019
Kasapkara, C. S. Et Al. 2019. When a common symptom of a neonate become an unusual diagnosis: A case report of HMG-CoA lyase deficiency with a novel mutation. Gazi Medical Journal , vol.30, no.3 , 298-299.
Kasapkara, C. S., Akar, M., Ozbek, M. N., Tuzun, H., Akcaboy, M., & CEYLANER, S., (2019). When a common symptom of a neonate become an unusual diagnosis: A case report of HMG-CoA lyase deficiency with a novel mutation. Gazi Medical Journal , vol.30, no.3, 298-299.
Kasapkara, Cigdem Et Al. "When a common symptom of a neonate become an unusual diagnosis: A case report of HMG-CoA lyase deficiency with a novel mutation," Gazi Medical Journal , vol.30, no.3, 298-299, 2019
Kasapkara, Cigdem S. Et Al. "When a common symptom of a neonate become an unusual diagnosis: A case report of HMG-CoA lyase deficiency with a novel mutation." Gazi Medical Journal , vol.30, no.3, pp.298-299, 2019
Kasapkara, C. S. Et Al. (2019) . "When a common symptom of a neonate become an unusual diagnosis: A case report of HMG-CoA lyase deficiency with a novel mutation." Gazi Medical Journal , vol.30, no.3, pp.298-299.
@article{article, author={Cigdem Seher Kasapkara Et Al. }, title={When a common symptom of a neonate become an unusual diagnosis: A case report of HMG-CoA lyase deficiency with a novel mutation}, journal={Gazi Medical Journal}, year=2019, pages={298-299} }