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Search on : DE MELLO, MARICILDA PALANDI [Author]
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 Guaragna-Filho, Guilherme et al. 46,XX DSD and Antley-Bixler syndrome due to novel mutations in the cytochrome P450 oxidoreductase gene. Arq Bras Endocrinol Metab, Nov 2012, vol.56, no.8, p.578-585. ISSN 0004-2730


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 Castro, Carla Cristina Telles de Sousa et al. Clinical and molecular spectrum of patients with 17β-hydroxysteroid dehydrogenase type 3 (17-β-HSD3) deficiency. Arq Bras Endocrinol Metab, Nov 2012, vol.56, no.8, p.533-539. ISSN 0004-2730


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 Guaragna, Mara Sanches et al. Frasier syndrome: four new cases with unusual presentations. Arq Bras Endocrinol Metab, Nov 2012, vol.56, no.8, p.525-532. ISSN 0004-2730


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 Soardi, Fernanda Caroline et al. Phenotypic variability in a family with x-linked adrenoleukodystrophy caused by the p.Trp132Ter mutation. Arq Bras Endocrinol Metab, Nov 2010, vol.54, no.8, p.738-743. ISSN 0004-2730


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 Barros, Beatriz Amstalden et al. A inclusão de novas técnicas de análise citogenética aperfeiçoou o diagnóstico cromossômico da síndrome de Turner. Arq Bras Endocrinol Metab, Dez 2009, vol.53, no.9, p.1137-1142. ISSN 0004-2730


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