Screening for GHR mutations in children with idiopathic short stature (ISS):: identification of two novel mutations (N103S and R368C) (2003)
- Authors:
- USP affiliated authors: MENDONCA, BERENICE BILHARINHO DE - FM ; ARNHOLD, IVO JORGE PRADO - FM ; LIN, CHIN AN - FM
- Unidade: FM
- Assunto: ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Publisher place: Philadelphia
- Date published: 2003
- Source:
- Título do periódico: Resumos
- Conference titles: ENDO - The Endocrine Society's Annual Meeting
-
ABNT
JORGE, Alexander A. et al. Screening for GHR mutations in children with idiopathic short stature (ISS):: identification of two novel mutations (N103S and R368C). 2003, Anais.. Philadelphia: Faculdade de Medicina, Universidade de São Paulo, 2003. . Acesso em: 26 abr. 2024. -
APA
Jorge, A. A., Lin, C. J., Souza, S. C. A. L., Arnhold, I. J. P., & Mendonça, B. B. (2003). Screening for GHR mutations in children with idiopathic short stature (ISS):: identification of two novel mutations (N103S and R368C). In Resumos. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Jorge AA, Lin CJ, Souza SCAL, Arnhold IJP, Mendonça BB. Screening for GHR mutations in children with idiopathic short stature (ISS):: identification of two novel mutations (N103S and R368C). Resumos. 2003 ;[citado 2024 abr. 26 ] -
Vancouver
Jorge AA, Lin CJ, Souza SCAL, Arnhold IJP, Mendonça BB. Screening for GHR mutations in children with idiopathic short stature (ISS):: identification of two novel mutations (N103S and R368C). Resumos. 2003 ;[citado 2024 abr. 26 ] - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
- Absense of duplication on DAX1 gene in patients with 46,XY sex reversal
- Crescimento linear e estatura final em crianças com tumores adrenais predominantemente virilizantes
- Absense of inactivating mutations and deletions of DAX1 gene in SRY negative 46,XX sex-reversed patients
- Heterogeneidade clínica e molecular do hipogonadismo hipogonadotrófico (HH): importância da avaliação do sistema olfatório no diagnóstico diferencial
- Number of CAG repeats in Exon 1 of androgen receptor gene is not related to gender identity in adult patients with male psudohermaphroditism and male transexualism
- Clinical, hormonal, behavioral, and genetic characteristics of androgen insensitibity syndrome in a brazilian cohort: five novel mutations in the androgen receptor gene
- Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue
- Three novel mutations in CYP21 gene in brazilian patients with the classical form of 21-hydroxylase deficiency due to founder effect
- Padrão de resposta do TSH após estímulo com TRH em pacientes com hipotireoidismo hipofisário devido a mutações nos genes HESX1, PROP1 e PIT1
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
