Kocagil, 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, no.4 , 1.

Kocagil, S., Şafak, İ. N., Saraç, E., Aydın, C., Artan, S., & Kırel, 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, no.4, 1.

Kocagil, 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, no.4, 1, 2023

Kocagil, 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, no.4, pp.1, 2023

Kocagil, 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, no.4, p.1.

@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={1} }