Mıhçı, E. Et Al. 2018. Analysis of RunX2 mutations in four Turkish patients with Cleidocranial Dysplasia. ESHG (2019) , (Milan, Italy), 350.

Mıhçı, E., Nur, B., Toylu, A., Karaman, V., & Uyguner, Z. O., (2018). Analysis of RunX2 mutations in four Turkish patients with Cleidocranial Dysplasia . ESHG (2019) (pp.350). Milan, Italy

Mıhçı, ERCAN Et Al. "Analysis of RunX2 mutations in four Turkish patients with Cleidocranial Dysplasia," ESHG (2019), Milan, Italy, 2018

Mıhçı, ERCAN Et Al. "Analysis of RunX2 mutations in four Turkish patients with Cleidocranial Dysplasia." ESHG (2019) , Milan, Italy, pp.350, 2018

Mıhçı, E. Et Al. (2018) . "Analysis of RunX2 mutations in four Turkish patients with Cleidocranial Dysplasia." ESHG (2019) , Milan, Italy, p.350.

@conferencepaper{conferencepaper, author={ERCAN MIHÇI Et Al. }, title={Analysis of RunX2 mutations in four Turkish patients with Cleidocranial Dysplasia}, congress name={ESHG (2019)}, city={Milan}, country={Italy}, year={2018}, pages={350} }