Association Study of GWAS-Derived Loci with Height in Brazilian Children: Importance of MAP3K3, MMP24 and IGF1R Polymorphisms for Height Variation (2015)
- Authors:
- USP affiliated authors: JORGE, ALEXANDER AUGUSTO DE LIMA - FM ; MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- DOI: 10.1159/000437324
- Subjects: CRIANÇAS; BRASILEIROS; VARIAÇÃO GENÉTICA; POLIMORFISMO
- Language: Inglês
- Imprenta:
- Source:
- Título: Hormone Research in Paediatrics
- ISSN: 1663-2818
- Volume/Número/Paginação/Ano: v. 84, n. 4, p. 248-253, 2015
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
FONTENELE, Eveline Gadelha Pereira et al. Association Study of GWAS-Derived Loci with Height in Brazilian Children: Importance of MAP3K3, MMP24 and IGF1R Polymorphisms for Height Variation. Hormone Research in Paediatrics, v. 84, n. 4, p. 248-253, 2015Tradução . . Disponível em: https://doi.org/10.1159/000437324. Acesso em: 12 fev. 2026. -
APA
Fontenele, E. G. P., Moraes, M. E. A. de, d’Alva, C. B., Pinheiro, D. P., Landim, S. A. S. P., Trarbach, E. B., et al. (2015). Association Study of GWAS-Derived Loci with Height in Brazilian Children: Importance of MAP3K3, MMP24 and IGF1R Polymorphisms for Height Variation. Hormone Research in Paediatrics, 84( 4), 248-253. doi:10.1159/000437324 -
NLM
Fontenele EGP, Moraes MEA de, d’Alva CB, Pinheiro DP, Landim SASP, Trarbach EB, Mendonca BB de, Jorge AAL. Association Study of GWAS-Derived Loci with Height in Brazilian Children: Importance of MAP3K3, MMP24 and IGF1R Polymorphisms for Height Variation [Internet]. Hormone Research in Paediatrics. 2015 ; 84( 4): 248-253.[citado 2026 fev. 12 ] Available from: https://doi.org/10.1159/000437324 -
Vancouver
Fontenele EGP, Moraes MEA de, d’Alva CB, Pinheiro DP, Landim SASP, Trarbach EB, Mendonca BB de, Jorge AAL. Association Study of GWAS-Derived Loci with Height in Brazilian Children: Importance of MAP3K3, MMP24 and IGF1R Polymorphisms for Height Variation [Internet]. Hormone Research in Paediatrics. 2015 ; 84( 4): 248-253.[citado 2026 fev. 12 ] Available from: https://doi.org/10.1159/000437324 - Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes
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- Novel Mutations (p.G6R and p.R511W) in IGF1R Gene in Children Born Small for Gestational Age (SGA) Without Catch-up Growth
- Growth Hormone (GH) Pharmacogenetics: Positive Influence of GH Receptor (GHR) Exon 3 Deleted Allele (d3) on First-year Growth Velocity and Final Height in Patients with Turner Syndrome (TS) Treated with Recombinant Human GH (rhGH)
- Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients
- The Sitting Height/Height Ratio for Age in Healthy and Short Individuals and Its Potential Role in Selecting Short Children for SHOX Analysis
- ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome
- Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations
- Evaluation of SHOX defects in the era of next-generation sequencing
- Genetic diagnosis of congenital hypopituitarism by a target gene panel: novel pathogenic variants in GLI2, OTX2 and GHRHR
Informações sobre o DOI: 10.1159/000437324 (Fonte: oaDOI API)
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