S. A. Iseri Et Al. , "Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophy," HUMAN GENETICS , vol.128, no.1, pp.51-60, 2010
Iseri, S. A. Et Al. 2010. Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophy. HUMAN GENETICS , vol.128, no.1 , 51-60.
Iseri, S. A., Wyatt, A. W., NUERNBERG, G., KLUCK, C., NUERNBERG, P., Holder, G. E., ... Blair, E.(2010). Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophy. HUMAN GENETICS , vol.128, no.1, 51-60.
Iseri, Sibel Et Al. "Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophy," HUMAN GENETICS , vol.128, no.1, 51-60, 2010
Iseri, Sibel A. Et Al. "Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophy." HUMAN GENETICS , vol.128, no.1, pp.51-60, 2010
Iseri, S. A. Et Al. (2010) . "Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophy." HUMAN GENETICS , vol.128, no.1, pp.51-60.
@article{article, author={Sibel Aylin UĞUR İŞERİ Et Al. }, title={Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophy}, journal={HUMAN GENETICS}, year=2010, pages={51-60} }