DOĞAN, M. E. And DÜNDAR, M. 2019. A de novo novel frameshift variant in the penultimate exon of FBN1 gene cause of rare Marfan lipodystrophy syndrome. 13th Balkan Congress of Human Genetics , 69.

DOĞAN, M. E., & DÜNDAR, M., (2019). A de novo novel frameshift variant in the penultimate exon of FBN1 gene cause of rare Marfan lipodystrophy syndrome . 13th Balkan Congress of Human Genetics (pp.69).

DOĞAN, MUHAMMET, And MUNİS DÜNDAR. "A de novo novel frameshift variant in the penultimate exon of FBN1 gene cause of rare Marfan lipodystrophy syndrome," 13th Balkan Congress of Human Genetics, 2019

DOĞAN, MUHAMMET E. And DÜNDAR, MUNİS. "A de novo novel frameshift variant in the penultimate exon of FBN1 gene cause of rare Marfan lipodystrophy syndrome." 13th Balkan Congress of Human Genetics , pp.69, 2019

DOĞAN, M. E. And DÜNDAR, M. (2019) . "A de novo novel frameshift variant in the penultimate exon of FBN1 gene cause of rare Marfan lipodystrophy syndrome." 13th Balkan Congress of Human Genetics , p.69.

@conferencepaper{conferencepaper, author={MUHAMMET ENSAR DOĞAN And author={MUNİS DÜNDAR}, title={A de novo novel frameshift variant in the penultimate exon of FBN1 gene cause of rare Marfan lipodystrophy syndrome}, congress name={13th Balkan Congress of Human Genetics}, city={}, country={}, year={2019}, pages={69} }