KOCAGİL, S. Et Al. 2023. Further Evidence for RFWD3 Gene Causing Fanconi Anemia Complementation Group W: Detailed Clinical Report of the Second Case in the Literature. MOLECULAR SYNDROMOLOGY , vol.14 , 509-515.

KOCAGİL, S., ŞAFAK, İ. N., SARAÇ, E., AYDIN, C., ARTAN, S., & KIREL, B., (2023). Further Evidence for RFWD3 Gene Causing Fanconi Anemia Complementation Group W: Detailed Clinical Report of the Second Case in the Literature. MOLECULAR SYNDROMOLOGY , vol.14, 509-515.

KOCAGİL, SİNEM Et Al. "Further Evidence for RFWD3 Gene Causing Fanconi Anemia Complementation Group W: Detailed Clinical Report of the Second Case in the Literature," MOLECULAR SYNDROMOLOGY , vol.14, 509-515, 2023

KOCAGİL, SİNEM Et Al. "Further Evidence for RFWD3 Gene Causing Fanconi Anemia Complementation Group W: Detailed Clinical Report of the Second Case in the Literature." MOLECULAR SYNDROMOLOGY , vol.14, pp.509-515, 2023

KOCAGİL, S. Et Al. (2023) . "Further Evidence for RFWD3 Gene Causing Fanconi Anemia Complementation Group W: Detailed Clinical Report of the Second Case in the Literature." MOLECULAR SYNDROMOLOGY , vol.14, pp.509-515.

@article{article, author={SİNEM KOCAGİL Et Al. }, title={Further Evidence for RFWD3 Gene Causing Fanconi Anemia Complementation Group W: Detailed Clinical Report of the Second Case in the Literature}, journal={MOLECULAR SYNDROMOLOGY}, year=2023, pages={509-515} }