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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. Contribuição da análise molecular do gene regulador da condutância transmembrana na fibrose cística na investigação diagnóstica de pacientes com suspeita de fibrose cística leve ou doença atípica. J. bras. pneumol., Abr 2013, vol.39, no.2, p.181-189. ISSN 1806-3713


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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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 Bressel, Tatiana A.B. et al. An effective device for generating alginate microcapsules. Genet. Mol. Biol., 2008, vol.31, no.1, p.136-140. ISSN 1415-4757
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 Lorenzoni, Paulo José et al. Niemann-Pick disease type C: a case series of Brazilian patients. Arq. Neuro-Psiquiatr., Mar 2014, vol.72, no.3, p.214-218. ISSN 0004-282X


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