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Search on : BRUNONI, DECIO [Author]
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 Mecca, Tatiana Pontrelli et al. Rastreamento de sinais e sintomas de transtornos do espectro do autismo em irmãos. Rev. psiquiatr. Rio Gd. Sul, 2011, vol.33, no.2, p.116-120. ISSN 0101-8108


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 Mesquita, Maria Luiza G. de et al. Fenótipo comportamental de crianças e adolescentes com síndrome de Prader-Willi. Rev. paul. pediatr., Mar 2010, vol.28, no.1, p.63-69. ISSN 0103-0582


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 Sato, Fábio Pinato et al. Instrument to screen cases of pervasive developmental disorder: a preliminary indication of validity. Rev. Bras. Psiquiatr., Mar 2009, vol.31, no.1, p.30-33. ISSN 1516-4446


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 Carvalheira, Gianna, Vergani, Naja and Brunoni, Décio Genética do autismo. Rev. Bras. Psiquiatr., Dez 2004, vol.26, no.4, p.270-272. ISSN 1516-4446


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 Porto, Marianna P.R. et al. Novel mutations in the TBX5 gene in patients with Holt-Oram Syndrome. Genet. Mol. Biol., 2010, vol.33, no.2, p.232-236. ISSN 1415-4757
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 Christofolini, Denise M. et al. Clinical checklists in the selection of mentally retarded males for molecular screening of fragile X syndrome. Genet. Mol. Biol., 2007, vol.30, no.4, p.1047-1050. ISSN 1415-4757
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 Longhitano, Silvia Bragagnolo and Brunoni, Décio Genetic hearing loss: a study of 228 Brazilian patients. Genet. Mol. Biol., Mar 2000, vol.23, no.1, p.25-27. ISSN 1415-4757


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 Galera, Marcial Francis et al. Clinical, genetical, radiological, and anatomopathological survey of 17 patients with lethal osteochondrodysplasias. Genet. Mol. Biol., June 1998, vol.21, no.2, p.267-272. ISSN 1415-4757


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 Brunoni, Décio. Aconselhamento Genético. Ciênc. saúde coletiva, 2002, vol.7, no.1, p.101-107. ISSN 1413-8123


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 Nicola, Pablo Domingos Rodrigues de et al. A utilização da Internet na notificação dos defeitos congênitos na Declaração de Nascido Vivo em quatro maternidades públicas do Município de São Paulo, Brasil. Cad. Saúde Pública, Jul 2010, vol.26, no.7, p.1383-1390. ISSN 0102-311X


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