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Search on : MARQUES-DE-FARIA, ANTONIA PAULA [Author]
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 Bley, Adriano Morad et al. Sexual difference, identification and object choice in individuals with sex differentiation disorders. Rev. latinoam. psicopatol. fundam., Sept 2012, vol.15, no.3, p.464-481. ISSN 1415-4714

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 Torres, Fábio Rossi et al. Estudos genéticos e moleculares em um grande grupo de pacientes com malformações do córtex cerebral. J. epilepsy clin. neurophysiol., Set 2008, vol.14, no.3, p.101-105. ISSN 1676-2649

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 Carvalho, Annelise B. et al. Síndrome de Turner: um diagnóstico pediátrico frequentemente realizado por não pediatras. J. Pediatr. (Rio J.), Abr 2010, vol.86, no.2, p.121-125. ISSN 0021-7557

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 Steiner, Carlos Eduardo, Cintra, Maria Letícia and Marques-de-Faria, Antonia Paula Cutis laxa with growth and developmental delay, wrinkly skin syndrome and gerodermia osteodysplastica: a report of two unrelated patients and a literature review. Genet. Mol. Biol., 2005, vol.28, no.2, p.181-190. ISSN 1415-4757
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 Oliveira, Gisele Viana de et al. Deafness, palmoplantar hyperkeratosis, and knuckle pads with male-to-male transmission: Bart-Pumphrey syndrome. Genet. Mol. Biol., 2003, vol.26, no.2, p.129-131. ISSN 1415-4757
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 Moraes, Ana Maria Silveira Machado de, Magna, Luís Alberto and Marques-de-Faria, Antonia Paula Prevenção da deficiência mental: conhecimento e percepção dos profissionais de saúde. Cad. Saúde Pública, Mar 2006, vol.22, no.3, p.685-690. ISSN 0102-311X

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 Steiner, Carlos Eduardo, Guerreiro, Marilisa Mantovani and Marques-de-Faria, Antonia Paula Genetic and neurological evaluation in a sample of individuals with pervasive developmental disorders. Arq. Neuro-Psiquiatr., June 2003, vol.61, no.2A, p.176-180. ISSN 0004-282X

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 Steiner, Carlos Eduardo et al. Genotype and natural history in unrelated individual with phenylketonuria and autistic behavior. Arq. Neuro-Psiquiatr., June 2007, vol.65, no.2A, p.202-205. ISSN 0004-282X

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 Steiner, Carlos Eduardo et al. Laboratorial diagnosis of fragile-X syndrome: experience in a sample of individuals with pervasive developmental disorders. Arq. Neuro-Psiquiatr., Sept 2005, vol.63, no.3a, p.564-570. ISSN 0004-282X

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 Rim, Priscila Hae Hyun et al. Ocular findings in Brazilian identical twins with Cohen syndrome: case report. Arq. Bras. Oftalmol., Dec 2009, vol.72, no.6, p.815-818. ISSN 0004-2749

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