Kutbay, N. O. Et Al. 2016. A case of familial partial lipodystrophy caused by a novel lamin A/C (LMNA) mutation in exon 1 (D47N). European Journal of Internal Medicine , vol.29 , 37-39.

Kutbay, N. O., Yurekli, B. S., Onay, H., ALTAY, C., Atik, T., HEKİMSOY, Z., ... Saygili, F.(2016). A case of familial partial lipodystrophy caused by a novel lamin A/C (LMNA) mutation in exon 1 (D47N). European Journal of Internal Medicine , vol.29, 37-39.

Kutbay, Nilufer Et Al. "A case of familial partial lipodystrophy caused by a novel lamin A/C (LMNA) mutation in exon 1 (D47N)," European Journal of Internal Medicine , vol.29, 37-39, 2016

Kutbay, Nilufer O. Et Al. "A case of familial partial lipodystrophy caused by a novel lamin A/C (LMNA) mutation in exon 1 (D47N)." European Journal of Internal Medicine , vol.29, pp.37-39, 2016

Kutbay, N. O. Et Al. (2016) . "A case of familial partial lipodystrophy caused by a novel lamin A/C (LMNA) mutation in exon 1 (D47N)." European Journal of Internal Medicine , vol.29, pp.37-39.

@article{article, author={Nilufer Ozdemir Kutbay Et Al. }, title={A case of familial partial lipodystrophy caused by a novel lamin A/C (LMNA) mutation in exon 1 (D47N)}, journal={European Journal of Internal Medicine}, year=2016, pages={37-39} }