Türkyilmaz, A. Et Al. 2022. Novel SH3PXD2B variant identified by whole-exome sequencing in a Turkish newborn with Frank-Ter Haar Syndrome.. Clinical dysmorphology , vol.31 , 45-49.

Türkyilmaz, A., Sager, S. G., Topcu, B., Kaplan, A. T., Günbey, H. P., & Akin, Y., (2022). Novel SH3PXD2B variant identified by whole-exome sequencing in a Turkish newborn with Frank-Ter Haar Syndrome.. Clinical dysmorphology , vol.31, 45-49.

Türkyilmaz, AYBERK Et Al. "Novel SH3PXD2B variant identified by whole-exome sequencing in a Turkish newborn with Frank-Ter Haar Syndrome.," Clinical dysmorphology , vol.31, 45-49, 2022

Türkyilmaz, AYBERK Et Al. "Novel SH3PXD2B variant identified by whole-exome sequencing in a Turkish newborn with Frank-Ter Haar Syndrome.." Clinical dysmorphology , vol.31, pp.45-49, 2022

Türkyilmaz, A. Et Al. (2022) . "Novel SH3PXD2B variant identified by whole-exome sequencing in a Turkish newborn with Frank-Ter Haar Syndrome.." Clinical dysmorphology , vol.31, pp.45-49.

@article{article, author={AYBERK TÜRKYILMAZ Et Al. }, title={Novel SH3PXD2B variant identified by whole-exome sequencing in a Turkish newborn with Frank-Ter Haar Syndrome.}, journal={Clinical dysmorphology}, year=2022, pages={45-49} }