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Search on : STEINER, CARLOS EDUARDO [Author]
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 Nogueira, Roberto José Negrão et al. Anthropometric and body-mass composition suggests an intrinsic feature in Williams-Beuren syndrome. Rev. Assoc. Med. Bras., Dec 2011, vol.57, no.6, p.681-685. ISSN 0104-4230


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 Dornelles, Alícia Dorneles et al. Enzyme replacement therapy for Mucopolysaccharidosis Type I among patients followed within the MPS Brazil Network. Genet. Mol. Biol., 2014, vol.37, no.1, p.23-29. ISSN 1415-4757
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 Steiner, Carlos Eduardo and Cavalcanti, Denise Pontes Christine Hackel (1955-2013). Genet. Mol. Biol., 2014, vol.37, no.1, p.v-v. ISSN 1415-4757
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 Carlin, Marcelo Paschoalete et al. Determining mutations in G6PC and SLC37A4 genes in a sample of Brazilian patients with glycogen storage disease types Ia and Ib. Genet. Mol. Biol., 2013, vol.36, no.4, p.502-506. ISSN 1415-4757
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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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 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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