Kaya, M. Et Al. 2022. Cytogenetic and molecular characterization of a patient having infertility and mild intellectual disability with a very rare unstable ring chromosome 13. SCOTTISH MEDICAL JOURNAL , vol.67, no.4 , 173-177.

Kaya, M., Suer, İ., Kalayci, T., Karaman, B., Ozturk, Ş., & Palanduz, Ş., (2022). Cytogenetic and molecular characterization of a patient having infertility and mild intellectual disability with a very rare unstable ring chromosome 13. SCOTTISH MEDICAL JOURNAL , vol.67, no.4, 173-177.

Kaya, Murat Et Al. "Cytogenetic and molecular characterization of a patient having infertility and mild intellectual disability with a very rare unstable ring chromosome 13," SCOTTISH MEDICAL JOURNAL , vol.67, no.4, 173-177, 2022

Kaya, Murat Et Al. "Cytogenetic and molecular characterization of a patient having infertility and mild intellectual disability with a very rare unstable ring chromosome 13." SCOTTISH MEDICAL JOURNAL , vol.67, no.4, pp.173-177, 2022

Kaya, M. Et Al. (2022) . "Cytogenetic and molecular characterization of a patient having infertility and mild intellectual disability with a very rare unstable ring chromosome 13." SCOTTISH MEDICAL JOURNAL , vol.67, no.4, pp.173-177.

@article{article, author={Murat KAYA Et Al. }, title={Cytogenetic and molecular characterization of a patient having infertility and mild intellectual disability with a very rare unstable ring chromosome 13}, journal={SCOTTISH MEDICAL JOURNAL}, year=2022, pages={173-177} }