Z. E. Taşkıran Et Al. , "Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome," American Journal Of Medical Genetics Part A , vol.173, no.12, pp.3143-3152, 2017
Taşkıran, Z. E. Et Al. 2017. Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome. American Journal Of Medical Genetics Part A , vol.173, no.12 , 3143-3152.
Taşkıran, Z. E., Karaosmanoğlu, B., Koşukcu, C., Akgün Doğan, Ö., Taylan Şekeroğlu, H., Şimşek Kiper, P. Ö., ... Ütine, G. E.(2017). Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome. American Journal Of Medical Genetics Part A , vol.173, no.12, 3143-3152.
Taşkıran, ZİHNİ Et Al. "Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome," American Journal Of Medical Genetics Part A , vol.173, no.12, 3143-3152, 2017
Taşkıran, ZİHNİ E. Et Al. "Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome." American Journal Of Medical Genetics Part A , vol.173, no.12, pp.3143-3152, 2017
Taşkıran, Z. E. Et Al. (2017) . "Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome." American Journal Of Medical Genetics Part A , vol.173, no.12, pp.3143-3152.
@article{article, author={ZİHNİ EKİM TAŞKIRAN Et Al. }, title={Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome}, journal={American Journal Of Medical Genetics Part A}, year=2017, pages={3143-3152} }