Meric, R. Et Al. 2021. A patient with mental retardation, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratodermia syndrome caused by AP1B1 gene variant. CLINICAL DYSMORPHOLOGY , vol.30, no.1 , 54-57.

Meric, R., Ercan-Sencicek, A. G., ULUDAĞ ALKAYA, D., Sahin, Y., Sar, M., Bilguvar, K., ... Tuysuz, B.(2021). A patient with mental retardation, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratodermia syndrome caused by AP1B1 gene variant. CLINICAL DYSMORPHOLOGY , vol.30, no.1, 54-57.

Meric, Ruya Et Al. "A patient with mental retardation, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratodermia syndrome caused by AP1B1 gene variant," CLINICAL DYSMORPHOLOGY , vol.30, no.1, 54-57, 2021

Meric, Ruya Et Al. "A patient with mental retardation, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratodermia syndrome caused by AP1B1 gene variant." CLINICAL DYSMORPHOLOGY , vol.30, no.1, pp.54-57, 2021

Meric, R. Et Al. (2021) . "A patient with mental retardation, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratodermia syndrome caused by AP1B1 gene variant." CLINICAL DYSMORPHOLOGY , vol.30, no.1, pp.54-57.

@article{article, author={Ruya Meric Et Al. }, title={A patient with mental retardation, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratodermia syndrome caused by AP1B1 gene variant}, journal={CLINICAL DYSMORPHOLOGY}, year=2021, pages={54-57} }