Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH) (2016)
- Authors:
- Moreira, Eloisa S
- Silva, Isabela M.W
- Lourenço, Naila Cristina Vilaça
- Moreira, Danielle P
- Ribeiro, Cintia M
- Martins, Ana Luiza B
- Griesi-Oliveira, Karina
- Lazar, Monize
- Costa, Sílvia S
- Naslavsky, Michel
- Rocha, Kátia M
- Aguena, Meire
- Fett-Conte, Agnes C
- Zatz, Mayana
- Rosenberg, Carla
- Zachi, Elaine C
- Bertola, Débora R
- Vadasz, Estevão
- Passos-Bueno, Maria Rita
- USP affiliated authors: LOURENÇO, NAILA CRISTINA VILAÇA - IB ; COSTA, SILVIA SOUZA DA - IB ; ROCHA, KATIA MARIA DA - IB ; ZATZ, MAYANA - IB ; ROSENBERG, CARLA - IB ; BERTOLA, DÉBORA ROMEO - IB ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB
- Unidade: IB
- DOI: 10.1016/j.rasd.2015.12.012
- Subjects: AUTISMO; DOENÇAS GENÉTICAS; SEQUENCIAMENTO GENÉTICO; SEQUENCIAMENTO GENÉTICO; INTERAÇÃO SOCIAL (COMPORTAMENTO SOCIAL); TRANSTORNOS GLOBAIS DO DESENVOLVIMENTO INFANTIL
- Language: Inglês
- Imprenta:
- Publisher place: Philadelphia
- Date published: 2016
- Source:
- Título: Research in Autism Spectrum Disorders
- ISSN: 1750-9467
- Volume/Número/Paginação/Ano: v. 23, p. 145-151, Mar. 2016
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: green
- Licença: other-oa
-
ABNT
MOREIRA, Eloisa S et al. Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH). Research in Autism Spectrum Disorders, v. 23, p. 145-151, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.rasd.2015.12.012. Acesso em: 28 dez. 2025. -
APA
Moreira, E. S., Silva, I. M. W., Lourenço, N. C. V., Moreira, D. P., Ribeiro, C. M., Martins, A. L. B., et al. (2016). Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH). Research in Autism Spectrum Disorders, 23, 145-151. doi:10.1016/j.rasd.2015.12.012 -
NLM
Moreira ES, Silva IMW, Lourenço NCV, Moreira DP, Ribeiro CM, Martins ALB, Griesi-Oliveira K, Lazar M, Costa SS, Naslavsky M, Rocha KM, Aguena M, Fett-Conte AC, Zatz M, Rosenberg C, Zachi EC, Bertola DR, Vadasz E, Passos-Bueno MR. Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH) [Internet]. Research in Autism Spectrum Disorders. 2016 ; 23 145-151.[citado 2025 dez. 28 ] Available from: https://doi.org/10.1016/j.rasd.2015.12.012 -
Vancouver
Moreira ES, Silva IMW, Lourenço NCV, Moreira DP, Ribeiro CM, Martins ALB, Griesi-Oliveira K, Lazar M, Costa SS, Naslavsky M, Rocha KM, Aguena M, Fett-Conte AC, Zatz M, Rosenberg C, Zachi EC, Bertola DR, Vadasz E, Passos-Bueno MR. Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH) [Internet]. Research in Autism Spectrum Disorders. 2016 ; 23 145-151.[citado 2025 dez. 28 ] Available from: https://doi.org/10.1016/j.rasd.2015.12.012 - Craniosynostosis in 10q26 deletion patients: a consequence of brain underdevelopment or altered suture biology?
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Informações sobre o DOI: 10.1016/j.rasd.2015.12.012 (Fonte: oaDOI API)
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