YILMAZ, M. Et Al. 2017. Next Generation Exome Sequencing in the Molecular Diagnosis of Primary Hypobetalipoproteinemias. 13th International Congress on Inborn Errors of Metabolism , (Brazil).

YILMAZ, M., tarugi, p., KÖR, D., di leo, e., BULUT, F. D., rabacchi, c., ... KILAVUZ, S.(2017). Next Generation Exome Sequencing in the Molecular Diagnosis of Primary Hypobetalipoproteinemias . 13th International Congress on Inborn Errors of Metabolism, Brazil

YILMAZ, MUSTAFA Et Al. "Next Generation Exome Sequencing in the Molecular Diagnosis of Primary Hypobetalipoproteinemias," 13th International Congress on Inborn Errors of Metabolism, Brazil, 2017

YILMAZ, MUSTAFA Et Al. "Next Generation Exome Sequencing in the Molecular Diagnosis of Primary Hypobetalipoproteinemias." 13th International Congress on Inborn Errors of Metabolism , Brazil, 2017

YILMAZ, M. Et Al. (2017) . "Next Generation Exome Sequencing in the Molecular Diagnosis of Primary Hypobetalipoproteinemias." 13th International Congress on Inborn Errors of Metabolism , Brazil.

@conferencepaper{conferencepaper, author={MUSTAFA YILMAZ Et Al. }, title={Next Generation Exome Sequencing in the Molecular Diagnosis of Primary Hypobetalipoproteinemias}, congress name={13th International Congress on Inborn Errors of Metabolism}, city={}, country={Brazil}, year={2017}}