A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability (2018)
- Authors:
- Autor USP: KIM, CHONG AE - FM
- Unidade: FM
- DOI: 10.1038/s41598-018-31754-2
- Subjects: RETARDO MENTAL; DOENÇAS GENÉTICAS; ESTUDOS MULTICÊNTRICOS; MICRORNAS
- Agências de fomento:
- Ministerio da Ciencia, Tecnologia, Inovacoes e Comunicacoes/Financiadora de Estudos e Projetos-Ciencia e Tecnologia - Infraestrura (MCTI/FINEP-CT-INFRA) - Sao Paulo [01/2011]
- Financiado pela FINEP
- Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
Processo FAPESP: 2012/25247-6 - Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
- Language: Inglês
- Imprenta:
- Source:
- Título: Scientific reports
- ISSN: 2045-2322
- Volume/Número/Paginação/Ano: v. 8, article ID 13382, 8p, 2018
- Este artigo possui versão em acesso aberto
- URL de acesso aberto
- PDF de acesso aberto
- Versão do Documento: Versão publicada (Published version)
-
Status: Artigo publicado em periódico de acesso aberto (Gold Open Access) -
ABNT
CERONI, J. R. M. e KIM, Chong Ae. A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability. Scientific reports, v. 8, 2018Tradução . . Disponível em: https://doi.org/10.1038/s41598-018-31754-2. Acesso em: 11 mar. 2026. -
APA
Ceroni, J. R. M., & Kim, C. A. (2018). A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability. Scientific reports, 8. doi:10.1038/s41598-018-31754-2 -
NLM
Ceroni JRM, Kim CA. A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability [Internet]. Scientific reports. 2018 ; 8[citado 2026 mar. 11 ] Available from: https://doi.org/10.1038/s41598-018-31754-2 -
Vancouver
Ceroni JRM, Kim CA. A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability [Internet]. Scientific reports. 2018 ; 8[citado 2026 mar. 11 ] Available from: https://doi.org/10.1038/s41598-018-31754-2 - NK and B cell deficiency in a MPS type II family with novel mutation in the IDS gene
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