S. Aylan Gelen Et Al. , "Autoimmune Hemolytic Anemia Due to Spondyloenchondrodysplasia with Spastic Paraparesis and Intracranial Calcification due to Mutation in ACP5," JOURNAL OF PEDIATRIC GENETICS , 2021
Aylan Gelen, S. Et Al. 2021. Autoimmune Hemolytic Anemia Due to Spondyloenchondrodysplasia with Spastic Paraparesis and Intracranial Calcification due to Mutation in ACP5. JOURNAL OF PEDIATRIC GENETICS .
Aylan Gelen, S., Kara, B., Eser Şimşek, I., Güngör, M., Zengin, E., & Sarper, N., (2021). Autoimmune Hemolytic Anemia Due to Spondyloenchondrodysplasia with Spastic Paraparesis and Intracranial Calcification due to Mutation in ACP5. JOURNAL OF PEDIATRIC GENETICS .
Aylan Gelen, SEMA Et Al. "Autoimmune Hemolytic Anemia Due to Spondyloenchondrodysplasia with Spastic Paraparesis and Intracranial Calcification due to Mutation in ACP5," JOURNAL OF PEDIATRIC GENETICS , 2021
Aylan Gelen, SEMA A. Et Al. "Autoimmune Hemolytic Anemia Due to Spondyloenchondrodysplasia with Spastic Paraparesis and Intracranial Calcification due to Mutation in ACP5." JOURNAL OF PEDIATRIC GENETICS , 2021
Aylan Gelen, S. Et Al. (2021) . "Autoimmune Hemolytic Anemia Due to Spondyloenchondrodysplasia with Spastic Paraparesis and Intracranial Calcification due to Mutation in ACP5." JOURNAL OF PEDIATRIC GENETICS .
@article{article, author={SEMA AYLAN GELEN Et Al. }, title={Autoimmune Hemolytic Anemia Due to Spondyloenchondrodysplasia with Spastic Paraparesis and Intracranial Calcification due to Mutation in ACP5}, journal={JOURNAL OF PEDIATRIC GENETICS}, year=2021}