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Search on : SOARDI, FERNANDA CAROLINE [Author]
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 Bezerra, Kaio Raffael Valotta et al. Contribution of rs1799998 polymorphism in CYP11B2 gene in susceptibility to preeclampsia. Rev. Bras. Saude Mater. Infant., June 2020, vol.20, no.2, p.467-471. ISSN 1519-3829


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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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 Lusa, Letícia Gori et al. Structural aspects of the p.P222Q homozygous mutation of HSD3B2 gene in a patient with congenital adrenal hyperplasia. Arq Bras Endocrinol Metab, Nov 2010, vol.54, no.8, p.768-774. ISSN 0004-2730


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 Fabbri, Helena Campos et al. Long-term follow-up of an 8-year-old boy with insulinoma as the first manifestation of a familial form of multiple endocrine neoplasia type 1. Arq Bras Endocrinol Metab, Nov 2010, vol.54, no.8, p.754-760. 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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 Soardi, Fernanda Caroline et al. Heterozygosis for CYP21A2 mutation considered as 21-hydroxylase deficiency in neonatal screening. Arq Bras Endocrinol Metab, Nov 2008, vol.52, no.8, p.1388-1392. ISSN 0004-2730


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 Macedo, Luciana Cosentino de et al. Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets. Arq Bras Endocrinol Metab, Nov 2008, vol.52, no.8, p.1244-1251. ISSN 0004-2730


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 Andrade, Juliana Gabriel R. de et al. Clinical and genetic findings of five patients with WT1-related disorders. Arq Bras Endocrinol Metab, Nov 2008, vol.52, no.8, p.1236-1243. ISSN 0004-2730


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 Guerra-Junior, Gil et al. Absence of mutations in Pax6 gene in three cases of Morning Glory syndrome associated with isolated growth hormone deficiency. Arq Bras Endocrinol Metab, Nov 2008, vol.52, no.8, p.1221-1227. ISSN 0004-2730


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