Mapping of mutan genes causing Waardenburg Syndrome in Indonesian families = Pemetaan Gen Mutan Penyebab Sindrom Waardenburg di Indonesia
ABSTRACT: Waardenburg Syndrome type 1 (WSl) is a significant cause of congenital deafness and hearing impairment in humans. WSl is an autosomal dominant mutation with extensive phenotypic variation observed both within and between families. The purpose of this research is to map of mutant genes caus...
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[Yogyakarta] : Universitas Gadjah Mada
1993
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