Integrative variation analysis reveals that a complex genotype may specify phenotype in siblings with Syndromic Autism Spectrum Disorder (2017)
- Authors:
- Reis, Viviane Neri de Souza
- Kitajima, João Paulo
- Tahira, Ana Carolina
- Feio-dos-Santos, Ana Cecília
- Fock, Rodrigo Ambrosio - Universidade Federal de São Paulo (UNIFESP)
- Lisboa, Bianca Cristina Garcia
- Simões, Sérgio Nery
- Krepischi, Ana Cristina Victorino
- Rosenberg, Carla
- Lourenço, Naila Cristina
- Passos-Bueno, Maria Rita
- Brentani, Helena
- 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: 04 nov. 2024. -
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 NC, 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 2024 nov. 04 ] 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 NC, 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 2024 nov. 04 ] Available from: https://doi.org/10.1371/journal.pone.0170386 - Craniosynostosis in 10q26 deletion patients: a consequence of brain underdevelopment or altered suture biology?
- Genome-wide DNA methylation profile of leukocytes from melanoma patients with and without CDKN2A mutations
- DNA methylation landscape of hepatoblastomas reveals arrest at early stages of liver differentiation and cancer-related alterations
- Co-expression network of neural-differentiation genes shows specific pattern in schizophrenia
- Cytogenetically visible inversions are formed by multiple molecular mechanisms
- LINE-1 hypermethylation in peripheral blood of cutaneous melanoma patients is associated with metastasis
- Rare germline copy number variations in hereditary cutaneous melanoma
- Lymphovascular invasion and histologic grade are associated with specific genomic profiles in invasive carcinomas of the breast
- Upregulated genes at 2q24 gains as candidate oncogenes in hepatoblastomas
- Low frequency of germline TERT and MITF mutations in Brazilian melanoma-prone patients
Informações sobre o DOI: 10.1371/journal.pone.0170386 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
