Vural, S. Et Al. 2017. Skin-Dominant Phenotype in a Patient with H Syndrome: Identification of a Novel Mutation in the SLC29A3 Gene. CYTOGENETIC AND GENOME RESEARCH , vol.151, no.4 , 186-190.

Vural, S., Ertop, P., Durmaz, C. D., ŞANLI, H., HEPER, A., KUNDAKCI, N., ... KARABULUT, H. G.(2017). Skin-Dominant Phenotype in a Patient with H Syndrome: Identification of a Novel Mutation in the SLC29A3 Gene. CYTOGENETIC AND GENOME RESEARCH , vol.151, no.4, 186-190.

Vural, Secil Et Al. "Skin-Dominant Phenotype in a Patient with H Syndrome: Identification of a Novel Mutation in the SLC29A3 Gene," CYTOGENETIC AND GENOME RESEARCH , vol.151, no.4, 186-190, 2017

Vural, Secil Et Al. "Skin-Dominant Phenotype in a Patient with H Syndrome: Identification of a Novel Mutation in the SLC29A3 Gene." CYTOGENETIC AND GENOME RESEARCH , vol.151, no.4, pp.186-190, 2017

Vural, S. Et Al. (2017) . "Skin-Dominant Phenotype in a Patient with H Syndrome: Identification of a Novel Mutation in the SLC29A3 Gene." CYTOGENETIC AND GENOME RESEARCH , vol.151, no.4, pp.186-190.

@article{article, author={Secil Vural Et Al. }, title={Skin-Dominant Phenotype in a Patient with H Syndrome: Identification of a Novel Mutation in the SLC29A3 Gene}, journal={CYTOGENETIC AND GENOME RESEARCH}, year=2017, pages={186-190} }