Y. ŞAHİN Et Al. , "A Novel Homozygous HOXB1 Mutation in a Turkish Family with Hereditary Congenital Facial Paresis," XII. Ulusal Tıbbi Genetik Kongresi , İzmir, Turkey, 2016
ŞAHİN, Y. Et Al. 2016. A Novel Homozygous HOXB1 Mutation in a Turkish Family with Hereditary Congenital Facial Paresis. XII. Ulusal Tıbbi Genetik Kongresi , (İzmir, Turkey).
ŞAHİN, Y., GÜNGÖR, O., AYAZ, A., GÜNGÖR, G., Şahin, B., YAYKAŞLI, K., ... CEYLANER, S.(2016). A Novel Homozygous HOXB1 Mutation in a Turkish Family with Hereditary Congenital Facial Paresis . XII. Ulusal Tıbbi Genetik Kongresi, İzmir, Turkey
ŞAHİN, YAVUZ Et Al. "A Novel Homozygous HOXB1 Mutation in a Turkish Family with Hereditary Congenital Facial Paresis," XII. Ulusal Tıbbi Genetik Kongresi, İzmir, Turkey, 2016
ŞAHİN, YAVUZ Et Al. "A Novel Homozygous HOXB1 Mutation in a Turkish Family with Hereditary Congenital Facial Paresis." XII. Ulusal Tıbbi Genetik Kongresi , İzmir, Turkey, 2016
ŞAHİN, Y. Et Al. (2016) . "A Novel Homozygous HOXB1 Mutation in a Turkish Family with Hereditary Congenital Facial Paresis." XII. Ulusal Tıbbi Genetik Kongresi , İzmir, Turkey.
@conferencepaper{conferencepaper, author={YAVUZ ŞAHİN Et Al. }, title={A Novel Homozygous HOXB1 Mutation in a Turkish Family with Hereditary Congenital Facial Paresis}, congress name={XII. Ulusal Tıbbi Genetik Kongresi}, city={İzmir}, country={Turkey}, year={2016}}