5 results on '"FLAGIELLO, LUISA"'
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2. Expressed STSs and transcription of human Xq28
3. Autosomal-dominant Retinitis Pigrnentosa Associated with an Arg-135-Trp Point Mutation of the Rhodopsin Gene
4. A synaptobrevin–like gene in the Xq28 pseudoautosomal region undergoes X inactivation
5. Ocular signs associated with a rhodopsin mutation (Cys-167 → Arg) in a family with autosomal dominant retinitis pigmentosa.
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