KAZIMLI, U. Et Al. 2019. A novel missense variant in the homogentisate 1,2-dioxygenase (HGD) gene in a patient with clinical symptoms of alkaptonuria.. 13th Balkan Congress of Human Genetics , (Edirne, Turkey), 166.

KAZIMLI, U., DOĞAN, M. E., BAYSAL, K., ÖZKUL, Y., ŞENEL, S., & DÜNDAR, M., (2019). A novel missense variant in the homogentisate 1,2-dioxygenase (HGD) gene in a patient with clinical symptoms of alkaptonuria. . 13th Balkan Congress of Human Genetics (pp.166). Edirne, Turkey

KAZIMLI, ULVİYYA Et Al. "A novel missense variant in the homogentisate 1,2-dioxygenase (HGD) gene in a patient with clinical symptoms of alkaptonuria.," 13th Balkan Congress of Human Genetics, Edirne, Turkey, 2019

KAZIMLI, ULVİYYA Et Al. "A novel missense variant in the homogentisate 1,2-dioxygenase (HGD) gene in a patient with clinical symptoms of alkaptonuria.." 13th Balkan Congress of Human Genetics , Edirne, Turkey, pp.166, 2019

KAZIMLI, U. Et Al. (2019) . "A novel missense variant in the homogentisate 1,2-dioxygenase (HGD) gene in a patient with clinical symptoms of alkaptonuria.." 13th Balkan Congress of Human Genetics , Edirne, Turkey, p.166.

@conferencepaper{conferencepaper, author={ULVİYYA KAZIMLI Et Al. }, title={A novel missense variant in the homogentisate 1,2-dioxygenase (HGD) gene in a patient with clinical symptoms of alkaptonuria.}, congress name={13th Balkan Congress of Human Genetics}, city={Edirne}, country={Turkey}, year={2019}, pages={166} }