Hormone resistance and short stature: a journey through the pathways of hormone signaling (2021)
- Authors:
- Autor USP: JORGE, ALEXANDER AUGUSTO DE LIMA - FM
- Unidade: FM
- DOI: 10.1016/j.mce.2021.111416
- Subjects: HORMÔNIO DO CRESCIMENTO; METABOLISMO; ESTATURA
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: Molecular and cellular endocrinology
- ISSN: 0303-7207
- Volume/Número/Paginação/Ano: v. 536, article ID 111416, 12p, 2021
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
SCALCO, Renata C et al. Hormone resistance and short stature: a journey through the pathways of hormone signaling. Molecular and cellular endocrinology, v. 536, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2021.111416. Acesso em: 25 fev. 2026. -
APA
Scalco, R. C., Correa, F. A., Dantas, N. C. B., Vasques, G. A., & Jorge, A. A. de L. (2021). Hormone resistance and short stature: a journey through the pathways of hormone signaling. Molecular and cellular endocrinology, 536. doi:10.1016/j.mce.2021.111416 -
NLM
Scalco RC, Correa FA, Dantas NCB, Vasques GA, Jorge AA de L. Hormone resistance and short stature: a journey through the pathways of hormone signaling [Internet]. Molecular and cellular endocrinology. 2021 ; 536[citado 2026 fev. 25 ] Available from: https://doi.org/10.1016/j.mce.2021.111416 -
Vancouver
Scalco RC, Correa FA, Dantas NCB, Vasques GA, Jorge AA de L. Hormone resistance and short stature: a journey through the pathways of hormone signaling [Internet]. Molecular and cellular endocrinology. 2021 ; 536[citado 2026 fev. 25 ] Available from: https://doi.org/10.1016/j.mce.2021.111416 - The E180splice mutation in the GHR gene causing Laron syndrome: Witness of a Sephardic Jewish exodus from the Iberian Peninsula to the New World?
- Clinical Characterization of Patients With Autosomal Dominant Short Stature due to Aggrecan Mutations
- Mutations in C-natriuretic peptide (NPPC): a novel cause of autosomal dominant short stature
- Aplicação da genética molecular no manejo dos distúrbios do crescimento
- Heterozygous Mutations in Natriuretic Peptide Receptor-B (NPR2) Gene as a Cause of Short Stature in Patients Initially Classified as Idiopathic Short Stature
- Development of a minimum dataset for the monitoring of recombinant human growth hormone (rhGH) therapy use in children with growth hormone deficiency (GHD) - a gloBE-reg initiative
- Clinical application of ACMG-AMP guidelines in HNF1A and GCK variants in a cohort of MODY families
- SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling
- Novel SUZ12 mutations in Weaver-like syndrome
- Clinical and molecular analysis of pubertal control in a cohort of silver-russel and temple syndromes patients
Informações sobre o DOI: 10.1016/j.mce.2021.111416 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
