SILAN, F. Et Al. 2018. Rare disease or rare diagnosed diseases: Blau syndrome with a rare mutation in exon 9 of NOD2 gene from Canakkale. European Biotechnology Congress , (Athens, Greece).

SILAN, F., Djurovic, J., Bir, F. D., SILAN, C., & ÖZDEMİR, Ö., (2018). Rare disease or rare diagnosed diseases: Blau syndrome with a rare mutation in exon 9 of NOD2 gene from Canakkale . European Biotechnology Congress, Athens, Greece

SILAN, FATMA Et Al. "Rare disease or rare diagnosed diseases: Blau syndrome with a rare mutation in exon 9 of NOD2 gene from Canakkale," European Biotechnology Congress, Athens, Greece, 2018

SILAN, FATMA Et Al. "Rare disease or rare diagnosed diseases: Blau syndrome with a rare mutation in exon 9 of NOD2 gene from Canakkale." European Biotechnology Congress , Athens, Greece, 2018

SILAN, F. Et Al. (2018) . "Rare disease or rare diagnosed diseases: Blau syndrome with a rare mutation in exon 9 of NOD2 gene from Canakkale." European Biotechnology Congress , Athens, Greece.

@conferencepaper{conferencepaper, author={FATMA SILAN Et Al. }, title={Rare disease or rare diagnosed diseases: Blau syndrome with a rare mutation in exon 9 of NOD2 gene from Canakkale}, congress name={European Biotechnology Congress}, city={Athens}, country={Greece}, year={2018}}