A. Gezdirici Et Al. , "Olmsted syndrome: a novel homozygous TRPV3 mutation with severe phenotype," European Society of Human Genetics (ESHG) Conference , Glasgow, United Kingdom, pp.104, 2015
Gezdirici, A. Et Al. 2015. Olmsted syndrome: a novel homozygous TRPV3 mutation with severe phenotype. European Society of Human Genetics (ESHG) Conference , (Glasgow, United Kingdom), 104.
Gezdirici, A., Bayram, Y., ENGİN, B., ÇELİK, U., Tomasz, G., DEMİRKESEN, C., ... Karaca, E.(2015). Olmsted syndrome: a novel homozygous TRPV3 mutation with severe phenotype . European Society of Human Genetics (ESHG) Conference (pp.104). Glasgow, United Kingdom
Gezdirici, Alper Et Al. "Olmsted syndrome: a novel homozygous TRPV3 mutation with severe phenotype," European Society of Human Genetics (ESHG) Conference, Glasgow, United Kingdom, 2015
Gezdirici, Alper Et Al. "Olmsted syndrome: a novel homozygous TRPV3 mutation with severe phenotype." European Society of Human Genetics (ESHG) Conference , Glasgow, United Kingdom, pp.104, 2015
Gezdirici, A. Et Al. (2015) . "Olmsted syndrome: a novel homozygous TRPV3 mutation with severe phenotype." European Society of Human Genetics (ESHG) Conference , Glasgow, United Kingdom, p.104.
@conferencepaper{conferencepaper, author={Alper Gezdirici Et Al. }, title={Olmsted syndrome: a novel homozygous TRPV3 mutation with severe phenotype}, congress name={European Society of Human Genetics (ESHG) Conference}, city={Glasgow}, country={United Kingdom}, year={2015}, pages={104} }