YİŞ, U. Et Al. 2015. A Novel Mutation in the Mitochondrial DNA Cytochrome b Gene (MTCYB) in a Patient with Prader Willi Syndrome. JOURNAL OF CHILD NEUROLOGY , vol.30, no.3 , 378-381.

YİŞ, U., EZGÜ, F. S., Karakaya, P., Polat, I., ARSLAN, N., ÇANKAYA, T., ... GİRAY BOZKAYA, Ö.(2015). A Novel Mutation in the Mitochondrial DNA Cytochrome b Gene (MTCYB) in a Patient with Prader Willi Syndrome. JOURNAL OF CHILD NEUROLOGY , vol.30, no.3, 378-381.

YİŞ, ULUÇ Et Al. "A Novel Mutation in the Mitochondrial DNA Cytochrome b Gene (MTCYB) in a Patient with Prader Willi Syndrome," JOURNAL OF CHILD NEUROLOGY , vol.30, no.3, 378-381, 2015

YİŞ, ULUÇ Et Al. "A Novel Mutation in the Mitochondrial DNA Cytochrome b Gene (MTCYB) in a Patient with Prader Willi Syndrome." JOURNAL OF CHILD NEUROLOGY , vol.30, no.3, pp.378-381, 2015

YİŞ, U. Et Al. (2015) . "A Novel Mutation in the Mitochondrial DNA Cytochrome b Gene (MTCYB) in a Patient with Prader Willi Syndrome." JOURNAL OF CHILD NEUROLOGY , vol.30, no.3, pp.378-381.

@article{article, author={ULUÇ YİŞ Et Al. }, title={A Novel Mutation in the Mitochondrial DNA Cytochrome b Gene (MTCYB) in a Patient with Prader Willi Syndrome}, journal={JOURNAL OF CHILD NEUROLOGY}, year=2015, pages={378-381} }