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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
    · abstract in english    · text in english


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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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 Lederman, Vivian Renne Gerber et al. Divorce in families of children with Down Syndrome or Rett Syndrome. Ciênc. saúde coletiva, May 2015, vol.20, no.5, p.1363-1369. ISSN 1413-8123


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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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