Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients (2013)
- Authors:
- USP affiliated authors: MENDONÇA, BERENICE BILHARINHO DE - FM ; JORGE, ALEXANDER AUGUSTO DE LIMA - FM
- Unidade: FM
- DOI: 10.1159/000353762
- Subjects: ENDOCRINOPATIAS; HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA); TRANSTORNOS DO CRESCIMENTO
- Language: Inglês
- Imprenta:
- Source:
- Título: Hormone Research in Paediatrics
- ISSN: 1663-2818
- Volume/Número/Paginação/Ano: v. 80, suppl. 1, p. 295, res. P2-d1-952, 2013
- Conference titles: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
LIDO, Andria C. V. et al. Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000353762. Acesso em: 12 fev. 2026. , 2013 -
APA
Lido, A. C. V., França, M. M., Otto, A. P., Carvalho, L. R., Mendonça, B. B. de, Arnhold, I. J. P., & Jorge, A. A. de L. (2013). Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. doi:10.1159/000353762 -
NLM
Lido ACV, França MM, Otto AP, Carvalho LR, Mendonça BB de, Arnhold IJP, Jorge AA de L. Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients [Internet]. Hormone Research in Paediatrics. 2013 ; 80 295.[citado 2026 fev. 12 ] Available from: https://doi.org/10.1159/000353762 -
Vancouver
Lido ACV, França MM, Otto AP, Carvalho LR, Mendonça BB de, Arnhold IJP, Jorge AA de L. Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients [Internet]. Hormone Research in Paediatrics. 2013 ; 80 295.[citado 2026 fev. 12 ] Available from: https://doi.org/10.1159/000353762 - Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes
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Informações sobre o DOI: 10.1159/000353762 (Fonte: oaDOI API)
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