A RARE CASE OF 14Q31 DELETION LOSS OF NRXN3 GENE IN PATIENT DIAGNOSED WITH AUTISM SPECTRUM DISORDER

KARADUMAN N., BAYRAMOV R., DOĞAN M. E., CERRAH GÜNEŞ M., HEJAZİ N., BÜYÜKOĞLAN R., ...More

ULUSLARARASI KATKILI GEVHER NESİBE TIP GÜNLERİ 2016, Turkey, 11 - 13 February 2016

  • Publication Type: Conference Paper
  • Country: Turkey
  • Erciyes University Affiliated: Yes