³í¹®1) Molecular Genetic Etiology and Revisiting the Middle Ear Surgery Outcomes of Branchio-Oto-Renal Syndrome: Experience in a Tertiary Referral Center
³í¹®2) Phenotypic and molecular basis of SIX1 variants linked to non‑syndromic deafness and atypical branchio‑otic syndrome in South Korea
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