Associated Papers
Otological manifestations in branchiootorenal spectrum disorder: A systematic review and meta-analysis.
Chen A et al.
Clinical Genetics, 2021
A de novo and novel mutation in the EYA1 gene in a Chinese child with branchio-oto-renal syndrome.
Li G et al.
Intractable & Rare Diseases Research, 2018
EYA1 and SIX1 gene mutations in Japanese patients with branchio-oto-renal (BOR) syndrome and related conditions.
Okada M et al.
Pediatric Nephrology (berlin, Germany), 2006
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