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1
Complete deletion of the PROP1 gene in two sibling with combined pituitary hormone deficiency (CPHD)
Complete deletion of the PROP1 gene in two sibling with combined pituitary hormone deficiency (CPHD)
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Complete deletion of the PROP1 gene in two sibling with combined pituitary hormone deficiency (CPHD)

M. G. Abrao L Carvalho; M. V Leite; M Nishi; A Barbosa; I. J. P Arnhold; B. B Mendonça; Annual Meeting of the Sociedad Latinoamericana de Endocrinologia Pediátrica (SLEP) (17. 2004 Angra dos Reis)

Journal of pediatric endocrinology and metabolism London v. 17, n. suppl.5, p. 1345, res. Poster 1, 2004

London 2004

Localização: FM - Fac. Medicina    (BCSEP 355 2004 ) e outros locais(Acessar)

2
GH-Releasing hormone receptor gene a novel splice-disrupting mutation and study of founder effects
GH-Releasing hormone receptor gene a novel splice-disrupting mutation and study of founder effects
Material Type:
Artigo 		Adicionar ao Meu Espaço

GH-Releasing hormone receptor gene a novel splice-disrupting mutation and study of founder effects

Suemi Marui Ericka b Trabach; Margaret C. S Boguszewski; Marcela M França; Alexander A. L Jorge; Hiroshi Inoue; Mirian Y Nishi; Luiz de Lacerda Filho; Manuel H Aguiar-Oliveira; Berenice B Mendonça; Ivo J. P Arnhold

Hormone research in paediatrics Basel v.78, n. 3, p. 165-172, 2012

Basel 2012

Localização: FM - Fac. Medicina    (BCSEP 334 2012 )(Acessar)

3
GH-Releasing hormone receptor gene a novel splice-disrupting mutation and study of founder effects
GH-Releasing hormone receptor gene a novel splice-disrupting mutation and study of founder effects
Material Type:
Artigo 		Adicionar ao Meu Espaço

GH-Releasing hormone receptor gene a novel splice-disrupting mutation and study of founder effects

Suemi Marui Ericka b Trabach; Margaret C. S Boguszewski; Marcela M França; Alexander A. L Jorge; Hiroshi Inoue; Mirian Y Nishi; Luiz de Lacerda Filho; Manuel H Aguiar-Oliveira; Berenice B Mendonça; Ivo J. P Arnhold

Hormone research in paediatrics Basel v.78, n. 3, p. 165-172, 2012

Basel 2012

Localização: FM - Fac. Medicina    (BCSEP 334 2012 )(Acessar)

4
Analyses of the GLI2 Gene in Patients with Congenital Isolated GH Deficiency (IGHD) or Associated to Other Pituitary Hormone Deficiencies (CPHD) Without Holoprosencephaly (HPE)
Analyses of the GLI2 Gene in Patients with Congenital Isolated GH Deficiency (IGHD) or Associated to Other Pituitary Hormone Deficiencies (CPHD) Without Holoprosencephaly (HPE)
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Analyses of the GLI2 Gene in Patients with Congenital Isolated GH Deficiency (IGHD) or Associated to Other Pituitary Hormone Deficiencies (CPHD) Without Holoprosencephaly (HPE)

M. França A Jorge; L Carvalho; A Otto; F Corrêa; E Costalonga Mendonça. B.; I Arnhold; Annual Meeting of the Sociedad Latino-Americana de Endocrinología Pediátrica (SLEP) (22. 2011 Cartagena de Indias, Colombia)

Hormone Research in Paediatrics Basel v. 76, n. suppl. 4, p. 1, res. 2, 2011

Basel 2011

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Deste Autor:

  1. Mendonça, B
  2. Arnhold, I
  3. Nishi, M
  4. Jorge, A
  5. França, M

Neste Assunto:

  1. Amplificação De Genes
  2. Genes (Análise)
  3. Receptores Hormonais
  4. Mutação Genética
  5. Dna (Análise)

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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