Aurora Arghir

ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 6

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Genes

Clinical case reports

This page only lists publications with an associated author ORCID identifier.

Publications

Sorina Mihaela Papuc, Alina Erbescu, Adelina Glangher, Ioana Streata, Anca-Lelia Riza, Magdalena Budisteanu, Aurora Arghir
Autistic Behavior as Novel Clinical Finding in OFD1 Syndrome. Genes 14 (2) (2023)
Sorina Mihaela Papuc, Alina Erbescu, Adelina Glangher, Ioana Streata, Anca-Lelia Riza, Magdalena Budisteanu, Aurora Arghir
Autistic Behavior as Novel Clinical Finding in OFD1 Syndrome. Genes 14 (2) (2023)
Sorina Mihaela Papuc, Alina Erbescu, Adelina Glangher, Ioana Streata, Anca-Lelia Riza, Magdalena Budisteanu, Aurora Arghir
Autistic Behavior as Novel Clinical Finding in OFD1 Syndrome. Genes 14 (2) (2023)
Sorina Mihaela Papuc, Alina Erbescu, Adelina Glangher, Ioana Streata, Anca-Lelia Riza, Magdalena Budisteanu, Aurora Arghir
Autistic Behavior as Novel Clinical Finding in OFD1 Syndrome. Genes 14 (2) (2023)
Magdalena Budisteanu, Sorina Mihaela Papuc, Ioana Streata, Mihai Cucu, Andrei Pirvu, Simona Serban-Sosoi, Alina Erbescu, Emanuela Andrei, Catrinel Iliescu, Doina Ioana, Emilia Severin, Mihai Ioana, Aurora Arghir
The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 Patients. Genes 12 (7) (2021)
Aurora Arghir, Sorina Mihaela Papuc, Andreea-Cristina Tutulan-Cunita, Alina Erbescu, Sara Loddo, Silvia Genovese, Laura Ciocca, Marina Goldoni, Carmelo Piscopo, Laura Bernardini, Antonio Novelli, Magdalena Budisteanu
Autism and severe clinical phenotype in a patient with 8p21.2p11.21 deletion: Case report and literature review. Clinical case reports 9 (1) (2020)

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Publication Activity (10 Years)

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Aurora Arghir