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Browsing by Author Bir, Firdevs Dincsoy

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Issue DateTitleAuthor(s)TypeМp-cat.
2019Blau syndrome with a rare mutation in exon 9 of NOD2 geneĐurović, Jelena  ; Silan, Fatma; Bir, Firdevs Dincsoy; Silan, Coskun; Albuz, Burcu; Ozdemir, OzturkArticle
22M22
2018Rare disease or rare diagnosed diseases: Blau syndrome with a rare mutation in exon 9 of NOD2 gene from CanakkaleSilan, Fatma; Djurovic, Jelena; Bir, Firdevs Dincsoy; Silan, Coskun; Ozdemir, OzturkConference Paper
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