Yalçınkaya, B. Et Al. 2024. Biallelic Deletion of PEX26 Exon 4 in a Boy with Phenotypic Features of both Zellweger Syndrome and Infantile Refsum Disease. Molecular Syndromology , vol.15, no.5 , 380-388.

Yalçınkaya, B., Sağlam, K., Terali, K., Tekin, E., Taslak, H., & Türkyılmaz, A., (2024). Biallelic Deletion of PEX26 Exon 4 in a Boy with Phenotypic Features of both Zellweger Syndrome and Infantile Refsum Disease. Molecular Syndromology , vol.15, no.5, 380-388.

Yalçınkaya, Burhanettin Et Al. "Biallelic Deletion of PEX26 Exon 4 in a Boy with Phenotypic Features of both Zellweger Syndrome and Infantile Refsum Disease," Molecular Syndromology , vol.15, no.5, 380-388, 2024

Yalçınkaya, Burhanettin Et Al. "Biallelic Deletion of PEX26 Exon 4 in a Boy with Phenotypic Features of both Zellweger Syndrome and Infantile Refsum Disease." Molecular Syndromology , vol.15, no.5, pp.380-388, 2024

Yalçınkaya, B. Et Al. (2024) . "Biallelic Deletion of PEX26 Exon 4 in a Boy with Phenotypic Features of both Zellweger Syndrome and Infantile Refsum Disease." Molecular Syndromology , vol.15, no.5, pp.380-388.

@article{article, author={Burhanettin Yalçınkaya Et Al. }, title={Biallelic Deletion of PEX26 Exon 4 in a Boy with Phenotypic Features of both Zellweger Syndrome and Infantile Refsum Disease}, journal={Molecular Syndromology}, year=2024, pages={380-388} }