Tuysuz, B. Et Al. 2022. Severe Phenotype in Patients with X-linked Hydrocephalus Caused by a Missense Mutation in L1CAM. TURKISH ARCHIVES OF PEDIATRICS , vol.57, no.5 , 521-525.

Tuysuz, B., Ercan-Sencicek, A. G., Ozer, E., Goc, N., Yalcinkaya, C., & Bilguvar, K., (2022). Severe Phenotype in Patients with X-linked Hydrocephalus Caused by a Missense Mutation in L1CAM. TURKISH ARCHIVES OF PEDIATRICS , vol.57, no.5, 521-525.

Tuysuz, Beyhan Et Al. "Severe Phenotype in Patients with X-linked Hydrocephalus Caused by a Missense Mutation in L1CAM," TURKISH ARCHIVES OF PEDIATRICS , vol.57, no.5, 521-525, 2022

Tuysuz, Beyhan Et Al. "Severe Phenotype in Patients with X-linked Hydrocephalus Caused by a Missense Mutation in L1CAM." TURKISH ARCHIVES OF PEDIATRICS , vol.57, no.5, pp.521-525, 2022

Tuysuz, B. Et Al. (2022) . "Severe Phenotype in Patients with X-linked Hydrocephalus Caused by a Missense Mutation in L1CAM." TURKISH ARCHIVES OF PEDIATRICS , vol.57, no.5, pp.521-525.

@article{article, author={Beyhan Tuysuz Et Al. }, title={Severe Phenotype in Patients with X-linked Hydrocephalus Caused by a Missense Mutation in L1CAM}, journal={TURKISH ARCHIVES OF PEDIATRICS}, year=2022, pages={521-525} }