Yeter, B. Et Al. 2025. Clinical and molecular results in 15 Turkish patients with Wiedemann-Steiner syndrome: identification of eight novel KMT2A variants and a case of dual molecular diagnosis in the CSNK2A1. European Journal of Pediatrics , vol.184, no.8 .

Yeter, B., Demirkol, Y. K., Usluer, E., Oğuz, S., Eser, M., Yarar, M. H., ... Canbek, S.(2025). Clinical and molecular results in 15 Turkish patients with Wiedemann-Steiner syndrome: identification of eight novel KMT2A variants and a case of dual molecular diagnosis in the CSNK2A1. European Journal of Pediatrics , vol.184, no.8.

Yeter, Burcu Et Al. "Clinical and molecular results in 15 Turkish patients with Wiedemann-Steiner syndrome: identification of eight novel KMT2A variants and a case of dual molecular diagnosis in the CSNK2A1," European Journal of Pediatrics , vol.184, no.8, 2025

Yeter, Burcu Et Al. "Clinical and molecular results in 15 Turkish patients with Wiedemann-Steiner syndrome: identification of eight novel KMT2A variants and a case of dual molecular diagnosis in the CSNK2A1." European Journal of Pediatrics , vol.184, no.8, 2025

Yeter, B. Et Al. (2025) . "Clinical and molecular results in 15 Turkish patients with Wiedemann-Steiner syndrome: identification of eight novel KMT2A variants and a case of dual molecular diagnosis in the CSNK2A1." European Journal of Pediatrics , vol.184, no.8.

@article{article, author={Burcu Yeter Et Al. }, title={Clinical and molecular results in 15 Turkish patients with Wiedemann-Steiner syndrome: identification of eight novel KMT2A variants and a case of dual molecular diagnosis in the CSNK2A1}, journal={European Journal of Pediatrics}, year=2025}