KARADUMAN, N. Et Al. 2016. A RARE CASE OF 14Q31 DELETION LOSS OF NRXN3 GENE IN PATIENT DIAGNOSED WITH AUTISM SPECTRUM DISORDER. ULUSLARARASI KATKILI GEVHER NESİBE TIP GÜNLERİ 2016 , (Turkey).

KARADUMAN, N., BAYRAMOV, R., DOĞAN, M. E., CERRAH GÜNEŞ, M., HEJAZİ, N., BÜYÜKOĞLAN, R., ... GÜNDÜZ, C.(2016). A RARE CASE OF 14Q31 DELETION LOSS OF NRXN3 GENE IN PATIENT DIAGNOSED WITH AUTISM SPECTRUM DISORDER . ULUSLARARASI KATKILI GEVHER NESİBE TIP GÜNLERİ 2016, Turkey

KARADUMAN, NESLİHAN Et Al. "A RARE CASE OF 14Q31 DELETION LOSS OF NRXN3 GENE IN PATIENT DIAGNOSED WITH AUTISM SPECTRUM DISORDER," ULUSLARARASI KATKILI GEVHER NESİBE TIP GÜNLERİ 2016, Turkey, 2016

KARADUMAN, NESLİHAN Et Al. "A RARE CASE OF 14Q31 DELETION LOSS OF NRXN3 GENE IN PATIENT DIAGNOSED WITH AUTISM SPECTRUM DISORDER." ULUSLARARASI KATKILI GEVHER NESİBE TIP GÜNLERİ 2016 , Turkey, 2016

KARADUMAN, N. Et Al. (2016) . "A RARE CASE OF 14Q31 DELETION LOSS OF NRXN3 GENE IN PATIENT DIAGNOSED WITH AUTISM SPECTRUM DISORDER." ULUSLARARASI KATKILI GEVHER NESİBE TIP GÜNLERİ 2016 , Turkey.

@conferencepaper{conferencepaper, author={NESLİHAN KARADUMAN Et Al. }, title={A RARE CASE OF 14Q31 DELETION LOSS OF NRXN3 GENE IN PATIENT DIAGNOSED WITH AUTISM SPECTRUM DISORDER}, congress name={ULUSLARARASI KATKILI GEVHER NESİBE TIP GÜNLERİ 2016}, city={}, country={Turkey}, year={2016}}