Ozturan, E. K. Et Al. 2022. A cause of familial central precocious puberty: A Novel variant in the DLK1 gene and low serum DLK1 levels. HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 2 , 351.

Ozturan, E. K., Karaman, V., Gelmez, M. Y., Yildiz, M., Poyrazoglu, Ş., Bas, F., ... Uyguner, Z. O.(2022). A cause of familial central precocious puberty: A Novel variant in the DLK1 gene and low serum DLK1 levels. HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 2, 351.

Ozturan, Esin Et Al. "A cause of familial central precocious puberty: A Novel variant in the DLK1 gene and low serum DLK1 levels," HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 2, 351, 2022

Ozturan, Esin K. Et Al. "A cause of familial central precocious puberty: A Novel variant in the DLK1 gene and low serum DLK1 levels." HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 2, pp.351, 2022

Ozturan, E. K. Et Al. (2022) . "A cause of familial central precocious puberty: A Novel variant in the DLK1 gene and low serum DLK1 levels." HORMONE RESEARCH IN PAEDIATRICS , no.SUPPL 2, p.351.

@article{article, author={Esin Karakilic Ozturan Et Al. }, title={A cause of familial central precocious puberty: A Novel variant in the DLK1 gene and low serum DLK1 levels}, journal={HORMONE RESEARCH IN PAEDIATRICS}, year=2022, pages={351} }