Simsek-Kiper, P. O. Et Al. 2019. A novel NKX3-2 mutation associated with perinatal lethal phenotype of spondylo-megaepiphyseal-metaphyseal dysplasia in a neonate. European Journal of Medical Genetics , vol.62, no.1 , 21-26.

Simsek-Kiper, P. O., KOŞUKCU, C., Akgun-Dogan, O., GÖÇMEN, R., ÜTİNE, G. E., SOYER, T., ... Korkmaz-Toygar, A.(2019). A novel NKX3-2 mutation associated with perinatal lethal phenotype of spondylo-megaepiphyseal-metaphyseal dysplasia in a neonate. European Journal of Medical Genetics , vol.62, no.1, 21-26.

Simsek-Kiper, PELİN Et Al. "A novel NKX3-2 mutation associated with perinatal lethal phenotype of spondylo-megaepiphyseal-metaphyseal dysplasia in a neonate," European Journal of Medical Genetics , vol.62, no.1, 21-26, 2019

Simsek-Kiper, PELİN Ö. Et Al. "A novel NKX3-2 mutation associated with perinatal lethal phenotype of spondylo-megaepiphyseal-metaphyseal dysplasia in a neonate." European Journal of Medical Genetics , vol.62, no.1, pp.21-26, 2019

Simsek-Kiper, P. O. Et Al. (2019) . "A novel NKX3-2 mutation associated with perinatal lethal phenotype of spondylo-megaepiphyseal-metaphyseal dysplasia in a neonate." European Journal of Medical Genetics , vol.62, no.1, pp.21-26.

@article{article, author={PELİN ÖZLEM ŞİMŞEK KİPER Et Al. }, title={A novel NKX3-2 mutation associated with perinatal lethal phenotype of spondylo-megaepiphyseal-metaphyseal dysplasia in a neonate}, journal={European Journal of Medical Genetics}, year=2019, pages={21-26} }