5 results on '"Sartorato, Edi Lúcia"'
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2. Type II autosomal recessive cutis laxa: Report of another patient and molecular studies concerning three candidate genes
3. Molecular genetics study of deafness in Brazil: 8-year experience
4. G59S mutation in theGJB2 (connexin 26) gene in a patient with Bart-Pumphrey syndrome
5. Determination of the frequency of the 35delG allele in Brazilian neonates
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