ŞİMŞEK KİPER, P. Ö. 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.

ŞİMŞEK KİPER, P. Ö., KOŞUKCU, C., Akgun-Dogan, Ö., 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.

ŞİMŞEK KİPER, 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

ŞİMŞEK KİPER, 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

ŞİMŞEK KİPER, P. Ö. 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} }