H. Özkalaycı And E. Bora, "A case with rare compound heterzygous FBN1 gene mutation," 13 th balkan congress of human genetics , Edirne, Turkey, pp.55, 2019
Özkalaycı, H. And Bora, E. 2019. A case with rare compound heterzygous FBN1 gene mutation. 13 th balkan congress of human genetics , (Edirne, Turkey), 55.
Özkalaycı, H., & Bora, E., (2019). A case with rare compound heterzygous FBN1 gene mutation . 13 th balkan congress of human genetics (pp.55). Edirne, Turkey
Özkalaycı, HANDE, And ELÇİN BORA. "A case with rare compound heterzygous FBN1 gene mutation," 13 th balkan congress of human genetics, Edirne, Turkey, 2019
Özkalaycı, HANDE And Bora, ELÇİN. "A case with rare compound heterzygous FBN1 gene mutation." 13 th balkan congress of human genetics , Edirne, Turkey, pp.55, 2019
Özkalaycı, H. And Bora, E. (2019) . "A case with rare compound heterzygous FBN1 gene mutation." 13 th balkan congress of human genetics , Edirne, Turkey, p.55.
@conferencepaper{conferencepaper, author={HANDE ÖZKALAYCI And author={ELÇİN BORA}, title={A case with rare compound heterzygous FBN1 gene mutation}, congress name={13 th balkan congress of human genetics}, city={Edirne}, country={Turkey}, year={2019}, pages={55} }