Integrative variation analysis reveals that a complex genotype may specify phenotype in siblings with Syndromic Autism Spectrum Disorder (2017)
- Authors:
- USP affiliated authors: KREPISCHI, ANA CRISTINA VICTORINO - IB ; ROSENBERG, CARLA - IB ; LOURENÇO, NAILA CRISTINA VILAÇA - IB ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; BRENTANI, HELENA PAULA - FM
- Unidades: IB; FM
- DOI: 10.1371/journal.pone.0170386
- Subjects: AUTISMO; ESPECTROS; SINAIS E SINTOMAS; DOENÇAS GENÉTICAS; GENÓTIPOS; FENÓTIPOS; TRANSTORNOS MENTAIS
- Language: Inglês
- Imprenta:
- Publisher place: San Francisco
- Date published: 2017
- Source:
- Status:
- Artigo publicado em periódico de acesso aberto (Gold Open Access)
- Versão do Documento:
- Versão publicada (Published version)
- Acessar versão aberta:
-
ABNT
REIS, Viviane Neri de Souza et al. Integrative variation analysis reveals that a complex genotype may specify phenotype in siblings with Syndromic Autism Spectrum Disorder. PLoS ONE, v. 12, n. Ja 2017, p. 1-22, 2017Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0170386. Acesso em: 02 abr. 2026. -
APA
Reis, V. N. de S., Kitajima, J. P., Tahira, A. C., Feio-dos-Santos, A. C., Fock, R. A., Lisboa, B. C. G., et al. (2017). Integrative variation analysis reveals that a complex genotype may specify phenotype in siblings with Syndromic Autism Spectrum Disorder. PLoS ONE, 12( Ja 2017), 1-22. doi:10.1371/journal.pone.0170386 -
NLM
Reis VN de S, Kitajima JP, Tahira AC, Feio-dos-Santos AC, Fock RA, Lisboa BCG, Simões SN, Krepischi ACV, Rosenberg C, Lourenço NCV, Passos-Bueno MR, Brentani H. Integrative variation analysis reveals that a complex genotype may specify phenotype in siblings with Syndromic Autism Spectrum Disorder [Internet]. PLoS ONE. 2017 ; 12( Ja 2017): 1-22.[citado 2026 abr. 02 ] Available from: https://doi.org/10.1371/journal.pone.0170386 -
Vancouver
Reis VN de S, Kitajima JP, Tahira AC, Feio-dos-Santos AC, Fock RA, Lisboa BCG, Simões SN, Krepischi ACV, Rosenberg C, Lourenço NCV, Passos-Bueno MR, Brentani H. Integrative variation analysis reveals that a complex genotype may specify phenotype in siblings with Syndromic Autism Spectrum Disorder [Internet]. PLoS ONE. 2017 ; 12( Ja 2017): 1-22.[citado 2026 abr. 02 ] Available from: https://doi.org/10.1371/journal.pone.0170386 - Craniosynostosis in 10q26 deletion patients: a consequence of brain underdevelopment or altered suture biology?
- DNA methylation landscape of hepatoblastomas reveals arrest at early stages of liver differentiation and cancer-related alterations
- Genome-wide DNA methylation profile of leukocytes from melanoma patients with and without CDKN2A mutations
- Lymphovascular invasion and histologic grade are associated with specific genomic profiles in invasive carcinomas of the breast
- Genetic testing for idiopathic intellectual disability: use of DNA extracted from saliva for SNP Genotyping
- LINE-1 hypermethylation in peripheral blood of cutaneous melanoma patients is associated with metastasis
- Cytogenetically visible inversions are formed by multiple molecular mechanisms
- Genotype–phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: natural history of a patient and review of the literature
- Identification of new promising germline variants in melanoma-prone patients
- Upregulated genes at 2q24 gains as candidate oncogenes in hepatoblastomas
Informações sobre a disponibilidade de versões do artigo em acesso aberto coletadas automaticamente via oaDOI API (Unpaywall).
Por se tratar de integração com serviço externo, podem existir diferentes versões do trabalho (como preprints ou postprints), que podem diferir da versão publicada.
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
