Yavaş, A. K. Et Al. 2024. Homozygous PGAP2 Mutation Causes Hyperphosphatasia with Mental Retardation Syndrome-3: Genetic and Clinical Evaluation of the Ultra-Rare Inherited Glycosylphosphatidylinositol Biosynthesis Defect. Molecular Syndromology .

Yavaş, A. K., Özbey, S. Z., Ergin, B., Ünal, Y., Bilginer Gürbüz, B., Karaatmaca, B., ... Özyürek, H.(2024). Homozygous PGAP2 Mutation Causes Hyperphosphatasia with Mental Retardation Syndrome-3: Genetic and Clinical Evaluation of the Ultra-Rare Inherited Glycosylphosphatidylinositol Biosynthesis Defect. Molecular Syndromology .

Yavaş, Aynur Et Al. "Homozygous PGAP2 Mutation Causes Hyperphosphatasia with Mental Retardation Syndrome-3: Genetic and Clinical Evaluation of the Ultra-Rare Inherited Glycosylphosphatidylinositol Biosynthesis Defect," Molecular Syndromology , 2024

Yavaş, Aynur K. Et Al. "Homozygous PGAP2 Mutation Causes Hyperphosphatasia with Mental Retardation Syndrome-3: Genetic and Clinical Evaluation of the Ultra-Rare Inherited Glycosylphosphatidylinositol Biosynthesis Defect." Molecular Syndromology , 2024

Yavaş, A. K. Et Al. (2024) . "Homozygous PGAP2 Mutation Causes Hyperphosphatasia with Mental Retardation Syndrome-3: Genetic and Clinical Evaluation of the Ultra-Rare Inherited Glycosylphosphatidylinositol Biosynthesis Defect." Molecular Syndromology .

@article{article, author={Aynur Küçükçongar Yavaş Et Al. }, title={Homozygous PGAP2 Mutation Causes Hyperphosphatasia with Mental Retardation Syndrome-3: Genetic and Clinical Evaluation of the Ultra-Rare Inherited Glycosylphosphatidylinositol Biosynthesis Defect}, journal={Molecular Syndromology}, year=2024}