Kesim, F. Y. Et Al. 2014. Whole genome SNP genotyping confirms segregation of Unverricht-Lundborg Disease (ULD) with a repeat expansion in CSTB on 21q in a large consanguineous family followed by a novel haplotype based approach identifying the parent of origin and carrier status in the child with Trisomy 21 under the age of onset for ULD.. European Human Genetics Conference, European Society of Human Genetics (ESHG) , (Milan, Italy), 1.

Kesim, F. Y., Tuncer Kılınç, F. N., Yücesan, E., Çavuşoğlu, K., Çalık, M., İşcan, A., ... Uğur İşeri, S. A.(2014). Whole genome SNP genotyping confirms segregation of Unverricht-Lundborg Disease (ULD) with a repeat expansion in CSTB on 21q in a large consanguineous family followed by a novel haplotype based approach identifying the parent of origin and carrier status in the child with Trisomy 21 under the age of onset for ULD. . European Human Genetics Conference, European Society of Human Genetics (ESHG) (pp.1). Milan, Italy

Kesim, Fatma Et Al. "Whole genome SNP genotyping confirms segregation of Unverricht-Lundborg Disease (ULD) with a repeat expansion in CSTB on 21q in a large consanguineous family followed by a novel haplotype based approach identifying the parent of origin and carrier status in the child with Trisomy 21 under the age of onset for ULD.," European Human Genetics Conference, European Society of Human Genetics (ESHG), Milan, Italy, 2014

Kesim, Fatma Y. Et Al. "Whole genome SNP genotyping confirms segregation of Unverricht-Lundborg Disease (ULD) with a repeat expansion in CSTB on 21q in a large consanguineous family followed by a novel haplotype based approach identifying the parent of origin and carrier status in the child with Trisomy 21 under the age of onset for ULD.." European Human Genetics Conference, European Society of Human Genetics (ESHG) , Milan, Italy, pp.1, 2014

Kesim, F. Y. Et Al. (2014) . "Whole genome SNP genotyping confirms segregation of Unverricht-Lundborg Disease (ULD) with a repeat expansion in CSTB on 21q in a large consanguineous family followed by a novel haplotype based approach identifying the parent of origin and carrier status in the child with Trisomy 21 under the age of onset for ULD.." European Human Genetics Conference, European Society of Human Genetics (ESHG) , Milan, Italy, p.1.

@conferencepaper{conferencepaper, author={Fatma Yeşim Kesim Et Al. }, title={Whole genome SNP genotyping confirms segregation of Unverricht-Lundborg Disease (ULD) with a repeat expansion in CSTB on 21q in a large consanguineous family followed by a novel haplotype based approach identifying the parent of origin and carrier status in the child with Trisomy 21 under the age of onset for ULD.}, congress name={European Human Genetics Conference, European Society of Human Genetics (ESHG)}, city={Milan}, country={Italy}, year={2014}, pages={1} }