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Search on : SARAIVA-PEREIRA, MARIA LUIZA [Author]
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 Tramontina, Juliana Fernandes et al. Brain-derived neurotrophic factor gene val66met polymorphism and executive functioning in patients with bipolar disorder. Rev. Bras. Psiquiatr., June 2009, vol.31, no.2, p.136-140. ISSN 1516-4446


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 Aguiar, Ernestina Silva de et al. GSTM1, GSTT1, and GSTP1 polymorphisms, breast cancer risk factors and mammographic density in women submitted to breast cancer screening. Rev. bras. epidemiol., June 2012, vol.15, no.2, p.246-255. ISSN 1415-790X


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 Giugliani, Luciana et al. Responsividade à tetrahidrobiopterina em pacientes com deficiência de fenilalanina hidroxilase. J. Pediatr. (Rio J.), Jun 2011, vol.87, no.3, p.245-251. ISSN 0021-7557


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 Dal'Maso, Vinícius Buaes et al. Diagnostic contribution of molecular analysis of the cystic fibrosis transmembrane conductance regulator gene in patients suspected of having mild or atypical cystic fibrosis. J. bras. pneumol., Apr 2013, vol.39, no.2, p.181-189. ISSN 1806-3713


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 Málaga, Diana Rojas et al. Sensitivity, advantages, limitations, and clinical utility of targeted next-generation sequencing panels for the diagnosis of selected lysosomal storage disorders. Genet. Mol. Biol., 2019, vol.42, no.1, suppl.1, p.197-206. ISSN 1415-4757
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 Furtado, Gabriel Vasata et al. State biomarkers for Machado Joseph disease: Validation, feasibility and responsiveness to change. Genet. Mol. Biol., 2019, vol.42, no.1, suppl.1, p.238-251. ISSN 1415-4757
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 Giugliani, Roberto et al. Population medical genetics: translating science to the community. Genet. Mol. Biol., 2019, vol.42, no.1, suppl.1, p.312-320. ISSN 1415-4757
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 Castilhos, Raphael Machado de et al. Minimal prevalence of Huntington’s disease in the South of Brazil and instability of the expanded CAG tract during intergenerational transmissions. Genet. Mol. Biol., 2019, no.ahead. ISSN 1415-4757
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 Godinho, Fernanda Marques de Souza et al. Molecular Analysis of Spinal Muscular Atrophy: a genotyping protocol based on TaqMan® real-time PCR. Genet. Mol. Biol., 2012, vol.35, no.4, suppl.1, p.955-959. ISSN 1415-4757
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 Artigalás, Osvaldo et al. A patient presenting a 22q13 deletion associated with an apparently balanced translocation t(16;22): an illustrative case in the investigation of patients with low ARSA activity. Genet. Mol. Biol., 2012, vol.35, no.2, p.424-427. ISSN 1415-4757
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