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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Maria Edna de Melo

Hospital das Clínicas

Universidade de São Paulo

SP, Brasil

[email]@usp.br

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Affiliations

Hospital das Clínicas, Universidade de São Paulo, SP, Brasil. 2008
Unidade de Endocrinologia do Desenvolvimento, Laboratorio de Hormonios e Genetica Molecular LIM 42, Disciplina de Endocrinologia - HCFMUSP, Brazil. 2007

References

Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene in a Brazilian family. Melo, M.E., Marui, S., Brito, V.N., Mancini, M.C., Mendonca, B.B., Knoepfelmacher, M. Arq. Bras. Endocrinol. Metabol (2008) [Pubmed]
Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe. Melo, M.E., Marui, S., Carvalho, L.R., Arnhold, I.J., Leite, C.C., Mendonça, B.B., Knoepfelmacher, M. Clin. Endocrinol. (Oxf) (2007) [Pubmed]