ŞENER, E. F. Et Al. 2012. Exome Sequencing Reveals a Novel Deletion in CC2D1A Gene in a Family with Autism and Non-Syndromic Mental Retardation.. Uluslararası Katılımlı 1. Otizm Kongresi , (Turkey), 1-2.

ŞENER, E. F., Bademci, G., Tekin, M., Diken, H. İ., & ÖZKUL, Y., (2012). Exome Sequencing Reveals a Novel Deletion in CC2D1A Gene in a Family with Autism and Non-Syndromic Mental Retardation. . Uluslararası Katılımlı 1. Otizm Kongresi (pp.1-2). , Turkey

ŞENER, ELİF Et Al. "Exome Sequencing Reveals a Novel Deletion in CC2D1A Gene in a Family with Autism and Non-Syndromic Mental Retardation.," Uluslararası Katılımlı 1. Otizm Kongresi, Turkey, 2012

ŞENER, ELİF F. Et Al. "Exome Sequencing Reveals a Novel Deletion in CC2D1A Gene in a Family with Autism and Non-Syndromic Mental Retardation.." Uluslararası Katılımlı 1. Otizm Kongresi , Turkey, pp.1-2, 2012

ŞENER, E. F. Et Al. (2012) . "Exome Sequencing Reveals a Novel Deletion in CC2D1A Gene in a Family with Autism and Non-Syndromic Mental Retardation.." Uluslararası Katılımlı 1. Otizm Kongresi , Turkey, pp.1-2.

@conferencepaper{conferencepaper, author={ELİF FUNDA ŞENER Et Al. }, title={Exome Sequencing Reveals a Novel Deletion in CC2D1A Gene in a Family with Autism and Non-Syndromic Mental Retardation.}, congress name={Uluslararası Katılımlı 1. Otizm Kongresi}, city={}, country={Turkey}, year={2012}, pages={1-2} }