Growth Standards of Patients With Noonan and Noonan-Like Syndromes With Mutations in the RAS/MAPK Pathway (2012)
- Authors:
- USP affiliated authors: MENDONÇA, BERENICE BILHARINHO DE - FM ; BERTOLA, DÉBORA ROMEO - IB ; JORGE, ALEXANDER AUGUSTO DE LIMA - FM
- Unidades: FM; IB
- DOI: 10.1002/ajmg.a.35519
- Subjects: NANISMO (ASPECTOS ANTROPOLÓGICOS;GENÉTICA); ANORMALIDADES CRANIOFACIAIS (GENÉTICA); BIOLOGIA MOLECULAR; ANTROPOMETRIA; HORMÔNIO DO CRESCIMENTO; ÍNDICE DE MASSA CORPORAL
- Language: Inglês
- Imprenta:
- Source:
- Título: American journal of medical genetics part. A
- ISSN: 1552-4825
- Volume/Número/Paginação/Ano: n. (online), p. 1-7, 2012
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
MALAQUIAS, Alexsandra C. et al. Growth Standards of Patients With Noonan and Noonan-Like Syndromes With Mutations in the RAS/MAPK Pathway. American journal of medical genetics part. A, n. (online), p. 1-7, 2012Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.35519/pdf. Acesso em: 27 fev. 2026. -
APA
Malaquias, A. C., Brasil, A. S., Pereira, A. C., Arnhold, I. J. P., Mendonça, B. B., Bertola, D. R., & Jorge, A. A. L. (2012). Growth Standards of Patients With Noonan and Noonan-Like Syndromes With Mutations in the RAS/MAPK Pathway. American journal of medical genetics part. A, ( (online), 1-7. doi:10.1002/ajmg.a.35519 -
NLM
Malaquias AC, Brasil AS, Pereira AC, Arnhold IJP, Mendonça BB, Bertola DR, Jorge AAL. Growth Standards of Patients With Noonan and Noonan-Like Syndromes With Mutations in the RAS/MAPK Pathway [Internet]. American journal of medical genetics part. A. 2012 ;( (online): 1-7.[citado 2026 fev. 27 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.35519/pdf -
Vancouver
Malaquias AC, Brasil AS, Pereira AC, Arnhold IJP, Mendonça BB, Bertola DR, Jorge AAL. Growth Standards of Patients With Noonan and Noonan-Like Syndromes With Mutations in the RAS/MAPK Pathway [Internet]. American journal of medical genetics part. A. 2012 ;( (online): 1-7.[citado 2026 fev. 27 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.35519/pdf - Tegumentary manifestations of Noonan and Noonan-related syndromes
- Six additional cases of SEDC due to the same and recurrent R989C mutation in the COL2A1 gene—the clinical and radiological follow-up [Carta]
- Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes
- Baixa estatura desproporcional por mutações no gene SHOX
- 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
Informações sobre o DOI: 10.1002/ajmg.a.35519 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
