Kaya, M. Et Al. 2019. Case Report: a novel chromosomal insertion, 46, XY, inv ins(18;2)(q11.2;q13q22), in a patient with infertility and mild intellectual disability.. F1000Research , vol.8 , 281.

Kaya, M., Suer, İ., Öztürk, Ş., ÇEFLE, K., Karaman, B., & Palanduz, Ş., (2019). Case Report: a novel chromosomal insertion, 46, XY, inv ins(18;2)(q11.2;q13q22), in a patient with infertility and mild intellectual disability.. F1000Research , vol.8, 281.

Kaya, Murat Et Al. "Case Report: a novel chromosomal insertion, 46, XY, inv ins(18;2)(q11.2;q13q22), in a patient with infertility and mild intellectual disability.," F1000Research , vol.8, 281, 2019

Kaya, Murat Et Al. "Case Report: a novel chromosomal insertion, 46, XY, inv ins(18;2)(q11.2;q13q22), in a patient with infertility and mild intellectual disability.." F1000Research , vol.8, pp.281, 2019

Kaya, M. Et Al. (2019) . "Case Report: a novel chromosomal insertion, 46, XY, inv ins(18;2)(q11.2;q13q22), in a patient with infertility and mild intellectual disability.." F1000Research , vol.8, p.281.

@article{article, author={Murat KAYA Et Al. }, title={Case Report: a novel chromosomal insertion, 46, XY, inv ins(18;2)(q11.2;q13q22), in a patient with infertility and mild intellectual disability.}, journal={F1000Research}, year=2019, pages={281} }