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

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Ericka Barbosa Trarbach

Unidade de Endocrinologia do Desenvolvimento

Laboratório de Hormônios e Genética Molecular/LIM42 da Disciplina de Endocrinologia do Hospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo

São Paulo

Brazil

[email]@hotmail.com

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Unidade de Endocrinologia do Desenvolvimento, Laboratório de Hormônios e Genética Molecular/LIM42 da Disciplina de Endocrinologia do Hospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil. 2010
  • Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo, Disciplina de Endocrinologia e Metabologia, Av Dr Enéas de Carvalho Aguiar, Brazil. 2006
  • Laboratório de Genética Humana, Centro de Biologia Molecular e Engenharia Genética (CBMEG), UNICAMP, Campinas, Brazil. 2005

References

  1. Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1. Trarbach, E.B., Teles, M.G., Costa, E.M., Abreu, A.P., Garmes, H.M., Guerra, G., Baptista, M.T., de Castro, M., Mendonca, B.B., Latronico, A.C. Clin. Endocrinol. (Oxf) (2010) [Pubmed]
  2. Novel fibroblast growth factor receptor 1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia. Trarbach, E.B., Costa, E.M., Versiani, B., de Castro, M., Baptista, M.T., Garmes, H.M., de Mendonca, B.B., Latronico, A.C. J. Clin. Endocrinol. Metab. (2006) [Pubmed]
  3. Molecular analysis of KAL-1, GnRH-R, NELF and EBF2 genes in a series of Kallmann syndrome and normosmic hypogonadotropic hypogonadism patients. Trarbach, E.B., Baptista, M.T., Garmes, H.M., Hackel, C. J. Endocrinol. (2005) [Pubmed]
 
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