TUĞ BOZDOĞAN, S. Et Al. 2019. A rare cause of mental retardation and epilepsy: pediatric patient with 22q duplication and 6p deletion. 5. ADANA GENETİK GÜNLERİ NÖROGENETİK SEMPOZYUMU , (Turkey), 28-31.

TUĞ BOZDOĞAN, S., PERK, P., ALTUNBAŞAK, Ş., & BİŞGİN, A., (2019). A rare cause of mental retardation and epilepsy: pediatric patient with 22q duplication and 6p deletion . 5. ADANA GENETİK GÜNLERİ NÖROGENETİK SEMPOZYUMU (pp.28-31). , Turkey

TUĞ BOZDOĞAN, SEVCAN Et Al. "A rare cause of mental retardation and epilepsy: pediatric patient with 22q duplication and 6p deletion," 5. ADANA GENETİK GÜNLERİ NÖROGENETİK SEMPOZYUMU, Turkey, 2019

TUĞ BOZDOĞAN, SEVCAN T. Et Al. "A rare cause of mental retardation and epilepsy: pediatric patient with 22q duplication and 6p deletion." 5. ADANA GENETİK GÜNLERİ NÖROGENETİK SEMPOZYUMU , Turkey, pp.28-31, 2019

TUĞ BOZDOĞAN, S. Et Al. (2019) . "A rare cause of mental retardation and epilepsy: pediatric patient with 22q duplication and 6p deletion." 5. ADANA GENETİK GÜNLERİ NÖROGENETİK SEMPOZYUMU , Turkey, pp.28-31.

@conferencepaper{conferencepaper, author={SEVCAN TUĞ BOZDOĞAN Et Al. }, title={A rare cause of mental retardation and epilepsy: pediatric patient with 22q duplication and 6p deletion}, congress name={5. ADANA GENETİK GÜNLERİ NÖROGENETİK SEMPOZYUMU}, city={}, country={Turkey}, year={2019}, pages={28-31} }