Çatlı, G. Et Al. 2015. A Case of Achondrogenesis Type 2/ Hypochondrogenesis Due to a De Novo Mutation in the COL2A1 Gene. 1. Ege Endocrinology and Genetics Symposium , (İzmir, Turkey), 80.

Çatlı, G., Abacı, A., Anık, A., Shaneen, R., Ünver Tuhan, H., Erçal, D., ... Böber, E.(2015). A Case of Achondrogenesis Type 2/ Hypochondrogenesis Due to a De Novo Mutation in the COL2A1 Gene . 1. Ege Endocrinology and Genetics Symposium (pp.80). İzmir, Turkey

Çatlı, Gönül Et Al. "A Case of Achondrogenesis Type 2/ Hypochondrogenesis Due to a De Novo Mutation in the COL2A1 Gene," 1. Ege Endocrinology and Genetics Symposium, İzmir, Turkey, 2015

Çatlı, Gönül Et Al. "A Case of Achondrogenesis Type 2/ Hypochondrogenesis Due to a De Novo Mutation in the COL2A1 Gene." 1. Ege Endocrinology and Genetics Symposium , İzmir, Turkey, pp.80, 2015

Çatlı, G. Et Al. (2015) . "A Case of Achondrogenesis Type 2/ Hypochondrogenesis Due to a De Novo Mutation in the COL2A1 Gene." 1. Ege Endocrinology and Genetics Symposium , İzmir, Turkey, p.80.

@conferencepaper{conferencepaper, author={Gönül Çatlı Et Al. }, title={A Case of Achondrogenesis Type 2/ Hypochondrogenesis Due to a De Novo Mutation in the COL2A1 Gene}, congress name={1. Ege Endocrinology and Genetics Symposium}, city={İzmir}, country={Turkey}, year={2015}, pages={80} }