Kurnaz, E. Et Al. 2019. Rare Cause of Infantile Hypercalcemia: A Novel Mutation in the SLC34A1 Gene. HORMONE RESEARCH IN PAEDIATRICS , vol.91, no.4 , 278-284.

Kurnaz, E., Erdeve, S. S., Cetinkaya, S., & AYCAN, Z., (2019). Rare Cause of Infantile Hypercalcemia: A Novel Mutation in the SLC34A1 Gene. HORMONE RESEARCH IN PAEDIATRICS , vol.91, no.4, 278-284.

Kurnaz, Erdal Et Al. "Rare Cause of Infantile Hypercalcemia: A Novel Mutation in the SLC34A1 Gene," HORMONE RESEARCH IN PAEDIATRICS , vol.91, no.4, 278-284, 2019

Kurnaz, Erdal Et Al. "Rare Cause of Infantile Hypercalcemia: A Novel Mutation in the SLC34A1 Gene." HORMONE RESEARCH IN PAEDIATRICS , vol.91, no.4, pp.278-284, 2019

Kurnaz, E. Et Al. (2019) . "Rare Cause of Infantile Hypercalcemia: A Novel Mutation in the SLC34A1 Gene." HORMONE RESEARCH IN PAEDIATRICS , vol.91, no.4, pp.278-284.

@article{article, author={Erdal Kurnaz Et Al. }, title={Rare Cause of Infantile Hypercalcemia: A Novel Mutation in the SLC34A1 Gene}, journal={HORMONE RESEARCH IN PAEDIATRICS}, year=2019, pages={278-284} }