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:
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
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: 28 dez. 2025. -
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 2025 dez. 28 ] 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 2025 dez. 28 ] Available from: https://doi.org/10.1371/journal.pone.0170386 - Genome-wide DNA methylation profile of leukocytes from melanoma patients with and without CDKN2A mutations
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Informações sobre o DOI: 10.1371/journal.pone.0170386 (Fonte: oaDOI API)
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