ŞİMŞEK KİPER, P. Ö. Et Al. 2011. A rare case of 2q37 microdeletion with Albright hereditary osteodystrophy-like phenotype. TURKISH JOURNAL OF PEDIATRICS , vol.53, no.5 , 558-560.

ŞİMŞEK KİPER, P. Ö., ÜTİNE, G. E., ALANAY, Y., Aktas, D., ALİKAŞİFOĞLU, M., & BODUROĞLU, O. K., (2011). A rare case of 2q37 microdeletion with Albright hereditary osteodystrophy-like phenotype. TURKISH JOURNAL OF PEDIATRICS , vol.53, no.5, 558-560.

ŞİMŞEK KİPER, PELİN Et Al. "A rare case of 2q37 microdeletion with Albright hereditary osteodystrophy-like phenotype," TURKISH JOURNAL OF PEDIATRICS , vol.53, no.5, 558-560, 2011

ŞİMŞEK KİPER, PELİN Ö. Et Al. "A rare case of 2q37 microdeletion with Albright hereditary osteodystrophy-like phenotype." TURKISH JOURNAL OF PEDIATRICS , vol.53, no.5, pp.558-560, 2011

ŞİMŞEK KİPER, P. Ö. Et Al. (2011) . "A rare case of 2q37 microdeletion with Albright hereditary osteodystrophy-like phenotype." TURKISH JOURNAL OF PEDIATRICS , vol.53, no.5, pp.558-560.

@article{article, author={PELİN ÖZLEM ŞİMŞEK KİPER Et Al. }, title={A rare case of 2q37 microdeletion with Albright hereditary osteodystrophy-like phenotype}, journal={TURKISH JOURNAL OF PEDIATRICS}, year=2011, pages={558-560} }