Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways (2014)
- Authors:
- USP affiliated authors: COSTA, SILVIA SOUZA DA - IB ; BERTOLA, DÉBORA ROMEO - IB ; ROSENBERG, CARLA - IB ; JORGE, ALEXANDER AUGUSTO DE LIMA - FM
- Unidades: IB; FM
- DOI: 10.1530/eje-14-0232
- Subjects: GENES; IDADE GESTACIONAL; CRESCIMENTO E DESENVOLVIMENTO
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: European Journal of Endocrinology
- ISSN: 0804-4643
- Volume/Número/Paginação/Ano: v. 171, n. 2, p. 253-262, 2014
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
CANTON, Ana P. M. et al. Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways. European Journal of Endocrinology, v. 171, n. 2, p. 253-262, 2014Tradução . . Disponível em: https://doi.org/10.1530/eje-14-0232. Acesso em: 28 set. 2024. -
APA
Canton, A. P. M., Costa, S. S., Rodrigues, T. C., Bertola, D. R., Malaquias, A. C., Correa, F. A., et al. (2014). Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways. European Journal of Endocrinology, 171( 2), 253-262. doi:10.1530/eje-14-0232 -
NLM
Canton APM, Costa SS, Rodrigues TC, Bertola DR, Malaquias AC, Correa FA, Arnhold IJP, Rosenberg C, Jorge AAL. Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways [Internet]. European Journal of Endocrinology. 2014 ; 171( 2): 253-262.[citado 2024 set. 28 ] Available from: https://doi.org/10.1530/eje-14-0232 -
Vancouver
Canton APM, Costa SS, Rodrigues TC, Bertola DR, Malaquias AC, Correa FA, Arnhold IJP, Rosenberg C, Jorge AAL. Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways [Internet]. European Journal of Endocrinology. 2014 ; 171( 2): 253-262.[citado 2024 set. 28 ] Available from: https://doi.org/10.1530/eje-14-0232 - Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH gene
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Informações sobre o DOI: 10.1530/eje-14-0232 (Fonte: oaDOI API)
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