kara, e. Et Al. 2022. A Very Rare Cause of Developmental Delay and Progressive Microcephaly: Serine Biosynthesis and Transport Defects.. Society for the Study of Inborn Errors of Metabolism Annual Symposium , (Sydney, Australia).

kara, e., KÖŞECİ, B., BURGAÇ, E., KAPLAN, İ., KOR, D., BULUT, F. D., ... GÜL MERT, G.(2022). A Very Rare Cause of Developmental Delay and Progressive Microcephaly: Serine Biosynthesis and Transport Defects. . Society for the Study of Inborn Errors of Metabolism Annual Symposium, Sydney, Australia

kara, esra Et Al. "A Very Rare Cause of Developmental Delay and Progressive Microcephaly: Serine Biosynthesis and Transport Defects.," Society for the Study of Inborn Errors of Metabolism Annual Symposium, Sydney, Australia, 2022

kara, esra Et Al. "A Very Rare Cause of Developmental Delay and Progressive Microcephaly: Serine Biosynthesis and Transport Defects.." Society for the Study of Inborn Errors of Metabolism Annual Symposium , Sydney, Australia, 2022

kara, e. Et Al. (2022) . "A Very Rare Cause of Developmental Delay and Progressive Microcephaly: Serine Biosynthesis and Transport Defects.." Society for the Study of Inborn Errors of Metabolism Annual Symposium , Sydney, Australia.

@conferencepaper{conferencepaper, author={esra kara Et Al. }, title={A Very Rare Cause of Developmental Delay and Progressive Microcephaly: Serine Biosynthesis and Transport Defects.}, congress name={Society for the Study of Inborn Errors of Metabolism Annual Symposium}, city={Sydney}, country={Australia}, year={2022}}