Keskin, M. Et Al. 2017. A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene. JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.9, no.1 , 91-94.

Keskin, M., Sahin, N. M., Kurnaz, E., Bayramoglu, E., Erdeve, S. S., AYCAN, Z., ... Cetinkaya, S.(2017). A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene. JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.9, no.1, 91-94.

Keskin, Meliksah Et Al. "A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene," JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.9, no.1, 91-94, 2017

Keskin, Meliksah Et Al. "A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene." JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.9, no.1, pp.91-94, 2017

Keskin, M. Et Al. (2017) . "A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene." JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.9, no.1, pp.91-94.

@article{article, author={Meliksah Keskin Et Al. }, title={A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene}, journal={JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY}, year=2017, pages={91-94} }