Associated Papers
Otofaciocervical Syndrome and Its Overlap with Branchiootorenal Spectrum: An Integrated Literature Analysis of EYA1-Related Disorders, Including a Novel Case with an 8q13.2q13.3 Deletion.
Graziani L et al.
Genes, 2025
EYA1-related disorders: two clinical cases and a literature review.
Castiglione A et al.
International Journal of Pediatric Otorhinolaryngology, 2014
A novel frameshift mutation in the EYA1 gene in a Korean family with branchio-oto-renal syndrome.
Lee JD et al.
Annals of Clinical and Laboratory Science, 2009
Novel EYA1 mutation in a Korean branchio-oto-renal syndrome family.
Lee KY et al.
International Journal of Pediatric Otorhinolaryngology, 2007
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