S. Acar Et Al. , "Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3," PLOS ONE , vol.13, no.3, 2018
Acar, S. Et Al. 2018. Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3. PLOS ONE , vol.13, no.3 .
Acar, S., Bin Essai, H. A., DEMİR, K., Al-Rijjal, R. A., Zou, M., ÇATLI, G., ... ANIK, A.(2018). Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3. PLOS ONE , vol.13, no.3.
Acar, Sezer Et Al. "Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3," PLOS ONE , vol.13, no.3, 2018
Acar, Sezer Et Al. "Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3." PLOS ONE , vol.13, no.3, 2018
Acar, S. Et Al. (2018) . "Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3." PLOS ONE , vol.13, no.3.
@article{article, author={Sezer Acar Et Al. }, title={Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3}, journal={PLOS ONE}, year=2018}