KOCAGİL, S. Et Al. 2020. A rare homozygous variant in CUL7 gene in two syblings with variable features of 3M syndrome. 14. ULUSAL TIBBİ GENETİK KONGRESİ“Uluslararası Katılımlı” , (Turkey).

KOCAGİL, S., KILIÇ YILDIRIM, G., & ARTAN, S., (2020). A rare homozygous variant in CUL7 gene in two syblings with variable features of 3M syndrome . 14. ULUSAL TIBBİ GENETİK KONGRESİ“Uluslararası Katılımlı”, Turkey

KOCAGİL, SİNEM, GONCA KILIÇ YILDIRIM, And SEVİLHAN ARTAN. "A rare homozygous variant in CUL7 gene in two syblings with variable features of 3M syndrome," 14. ULUSAL TIBBİ GENETİK KONGRESİ“Uluslararası Katılımlı”, Turkey, 2020

KOCAGİL, SİNEM Et Al. "A rare homozygous variant in CUL7 gene in two syblings with variable features of 3M syndrome." 14. ULUSAL TIBBİ GENETİK KONGRESİ“Uluslararası Katılımlı” , Turkey, 2020

KOCAGİL, S. KILIÇ YILDIRIM, G. And ARTAN, S. (2020) . "A rare homozygous variant in CUL7 gene in two syblings with variable features of 3M syndrome." 14. ULUSAL TIBBİ GENETİK KONGRESİ“Uluslararası Katılımlı” , Turkey.

@conferencepaper{conferencepaper, author={SİNEM KOCAGİL Et Al. }, title={A rare homozygous variant in CUL7 gene in two syblings with variable features of 3M syndrome}, congress name={14. ULUSAL TIBBİ GENETİK KONGRESİ“Uluslararası Katılımlı”}, city={}, country={Turkey}, year={2020}}