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)
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)
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)
Intragenic delection of the shox gene in a family with Léri-Well dyschondrosteosis detected by multiplex ligation-dependent probe amplification (MLPA)
M. F. A. Funari A. A. L Jorge; I. J. P Arnhold; E. M Pinto; B. B Mendonça Nishi. M. Y.; International Congress of Endocrinology 2008 (13. Rio de Janeiro)
Arquivos Brasileiros de Endocrinologia e Metabologia São Paulo v. 52, supl. 6, parte II, p. S794, res. OP-097, 2008
São Paulo 2008
Localização:
FM - Fac. Medicina
(BCSEP 382 2008 )(Acessar)