Mengen, E. Et Al. 2017. AN INFANTILE HYPOPHOSPHATASIA CASE DUE TO A NOVEL MUTATION IN TNSALP GENE. HORMONE RESEARCH IN PAEDIATRICS , vol.88 , 91-92.

Mengen, E., KOTAN, L. D., Topaloglu, K., & YÜKSEL, B., (2017). AN INFANTILE HYPOPHOSPHATASIA CASE DUE TO A NOVEL MUTATION IN TNSALP GENE. HORMONE RESEARCH IN PAEDIATRICS , vol.88, 91-92.

Mengen, Eda Et Al. "AN INFANTILE HYPOPHOSPHATASIA CASE DUE TO A NOVEL MUTATION IN TNSALP GENE," HORMONE RESEARCH IN PAEDIATRICS , vol.88, 91-92, 2017

Mengen, Eda Et Al. "AN INFANTILE HYPOPHOSPHATASIA CASE DUE TO A NOVEL MUTATION IN TNSALP GENE." HORMONE RESEARCH IN PAEDIATRICS , vol.88, pp.91-92, 2017

Mengen, E. Et Al. (2017) . "AN INFANTILE HYPOPHOSPHATASIA CASE DUE TO A NOVEL MUTATION IN TNSALP GENE." HORMONE RESEARCH IN PAEDIATRICS , vol.88, pp.91-92.

@article{article, author={Eda Mengen Et Al. }, title={AN INFANTILE HYPOPHOSPHATASIA CASE DUE TO A NOVEL MUTATION IN TNSALP GENE}, journal={HORMONE RESEARCH IN PAEDIATRICS}, year=2017, pages={91-92} }