Analisis mutasi gen pax3 dan gen mitf pada penderita sindroma waarden burg di Indonesia=Mutation analysis of PAX3 and MITF eves in Indonesian Waardenburg Syndrome family
ABSTRACT Waardenburg syndrome (WS) is an autosomal dominant disorder characterized by dystopia canthorum, pigmentary disturbance of skin, hair and eye and sensorineural deafness. The basis for the phenotypic variability observed among and between WS families is unknown. In order to understand the mo...
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[Yogyakarta] : Universitas Gadjah Mada
1998
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