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• W2058642876 abstract "Branchiootorenal syndrome is an autosomal dominant disorder that affects an estimated 2% of profoundly deaf children. In addition to hearing impairment, it is characterized by a lop-ear deformity, preauricular pits, branchial cleft sinus tracts, and renal anomalies. The pathogenesis of the disease remains unknown; however, the defective gene has been localized to chromosome 8q by family linkage studies." @default.
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• W2058642876 date "1992-12-01" @default.
• W2058642876 modified "2023-09-27" @default.
• W2058642876 title "Localization of the gene for branchiootorenal syndrome to chromosome 8q" @default.
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• W2058642876 doi "https://doi.org/10.1016/s0888-7543(05)80102-8" @default.
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