B. Yalçınkaya Et Al. , "Biallelic Deletion of PEX26 Exon 4 in a Boy with Phenotypic Features of both Zellweger Syndrome and Infantile Refsum Disease," Molecular Syndromology , 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 .
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 .
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 , 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 , 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 .
@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}