Per, H. 2024. A novel pathogenic variant in VARS1 associated with a syndromic neurodevelopmental disorder with craniofacial, and neuroradiological abnormalities in a Turkish family. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.32, no.1 , 207-208.

Per, H., (2024). A novel pathogenic variant in VARS1 associated with a syndromic neurodevelopmental disorder with craniofacial, and neuroradiological abnormalities in a Turkish family. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.32, no.1, 207-208.

Per, HÜSEYİN. "A novel pathogenic variant in VARS1 associated with a syndromic neurodevelopmental disorder with craniofacial, and neuroradiological abnormalities in a Turkish family," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.32, no.1, 207-208, 2024

Per, HÜSEYİN. "A novel pathogenic variant in VARS1 associated with a syndromic neurodevelopmental disorder with craniofacial, and neuroradiological abnormalities in a Turkish family." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.32, no.1, pp.207-208, 2024

Per, H. (2024) . "A novel pathogenic variant in VARS1 associated with a syndromic neurodevelopmental disorder with craniofacial, and neuroradiological abnormalities in a Turkish family." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.32, no.1, pp.207-208.

@article{article, author={HÜSEYİN PER}, title={A novel pathogenic variant in VARS1 associated with a syndromic neurodevelopmental disorder with craniofacial, and neuroradiological abnormalities in a Turkish family}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2024, pages={207-208} }