DEMİR, K. Et Al. 2013. Severe short stature due to 3-M syndrome with a novel OBSL1 gene mutation. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.26 , 147-150.

DEMİR, K., Altincik, A., & BÖBER, E., (2013). Severe short stature due to 3-M syndrome with a novel OBSL1 gene mutation. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.26, 147-150.

DEMİR, KORCAN, Ayca Altincik, And ECE BÖBER. "Severe short stature due to 3-M syndrome with a novel OBSL1 gene mutation," JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.26, 147-150, 2013

DEMİR, KORCAN Et Al. "Severe short stature due to 3-M syndrome with a novel OBSL1 gene mutation." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.26, pp.147-150, 2013

DEMİR, K. Altincik, A. And BÖBER, E. (2013) . "Severe short stature due to 3-M syndrome with a novel OBSL1 gene mutation." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.26, pp.147-150.

@article{article, author={KORCAN DEMİR Et Al. }, title={Severe short stature due to 3-M syndrome with a novel OBSL1 gene mutation}, journal={JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM}, year=2013, pages={147-150} }