Keskin, M. Et Al. 2016. A Rare Cause of Short Stature: Patient with 3M Syndrome Revealed a New Mutation in Osbl1 Gene. HORMONE RESEARCH IN PAEDIATRICS , vol.86 , 470.

Keskin, M., Sahin, N. M., Kurnaz, E., Bayramoglu, E., Erdeve, S. S., AYCAN, Z., ... Cetinkaya, S.(2016). A Rare Cause of Short Stature: Patient with 3M Syndrome Revealed a New Mutation in Osbl1 Gene. HORMONE RESEARCH IN PAEDIATRICS , vol.86, 470.

Keskin, Meliksah Et Al. "A Rare Cause of Short Stature: Patient with 3M Syndrome Revealed a New Mutation in Osbl1 Gene," HORMONE RESEARCH IN PAEDIATRICS , vol.86, 470, 2016

Keskin, Meliksah Et Al. "A Rare Cause of Short Stature: Patient with 3M Syndrome Revealed a New Mutation in Osbl1 Gene." HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.470, 2016

Keskin, M. Et Al. (2016) . "A Rare Cause of Short Stature: Patient with 3M Syndrome Revealed a New Mutation in Osbl1 Gene." HORMONE RESEARCH IN PAEDIATRICS , vol.86, p.470.

@article{article, author={Meliksah Keskin Et Al. }, title={A Rare Cause of Short Stature: Patient with 3M Syndrome Revealed a New Mutation in Osbl1 Gene}, journal={HORMONE RESEARCH IN PAEDIATRICS}, year=2016, pages={470} }