Analysis of potential disease-causing variants in a patient with intellectual disability via whole-exome sequencing (2019)
- Authors:
- Ruy, Patricia de Cássia
- Barros, Isabela Ichihara
- Rosa, Reginaldo Cruz Alves
- Plaça, Jessica Rodrigues
- Corveloni, Amanda Cristina
- Cardoso, Cibele
- Souza, Aline Fernanda de
- Biagi Junior, Carlos Alberto Oliveira de
- Siena, Ádamo Davi Diogenes
- Zueli, Kamila Peronni
- Tellechea, Maria Florencia
- Carvalho, Simone da Costa e Silva
- Molfetta, Greice Andreotti de
- Pina Neto, João Monteiro de
- Silva Junior, Wilson Araújo da
- USP affiliated authors: MOLFETTA, GREICE ANDREOTTI DE - FMRP ; PINA NETO, JOÃO MONTEIRO DE - FMRP ; SILVA JUNIOR, WILSON ARAÚJO DA - FMRP ; CARVALHO, SIMONE DA COSTA E SILVA - FMRP ; BARROS, ISABELA ICHIHARA DE - FMRP ; ROSA, REGINALDO CRUZ ALVES - FMRP ; PLAÇA, JESSICA RODRIGUES - FMRP ; CORVELONI, AMANDA CRISTINA - FMRP ; CARDOSO, CIBELE - FMRP ; SOUZA, ALINE FERNANDA DE - FZEA ; BIAGI JÚNIOR, CARLOS ALBERTO OLIVEIRA DE - FMRP ; SIENA, ÁDAMO DAVI DIÓGENES - FMRP ; TELLECHEA, MARIA FLORENCIA - FMRP
- Unidades: FMRP; FZEA
- Subjects: SEQUENCIAMENTO GENÉTICO; PESSOAS COM DEFICIÊNCIA INTELECTUAL
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher: Associação Brasileira de Bioinformática e Biologia Computacional
- Publisher place: Campos do Jordão
- Date published: 2019
- Source:
- Título do periódico: Proceedings
- Conference titles: X-Meeting International Conference of the AB3C
-
ABNT
RUY, Patricia de Cássia et al. Analysis of potential disease-causing variants in a patient with intellectual disability via whole-exome sequencing. 2019, Anais.. Campos do Jordão: Associação Brasileira de Bioinformática e Biologia Computacional, 2019. Disponível em: http://drive.ab3c.org.br/index.php/s/WDdbkSCMs5onm49. Acesso em: 18 abr. 2024. -
APA
Ruy, P. de C., Barros, I. I., Rosa, R. C. A., Plaça, J. R., Corveloni, A. C., Cardoso, C., et al. (2019). Analysis of potential disease-causing variants in a patient with intellectual disability via whole-exome sequencing. In Proceedings. Campos do Jordão: Associação Brasileira de Bioinformática e Biologia Computacional. Recuperado de http://drive.ab3c.org.br/index.php/s/WDdbkSCMs5onm49 -
NLM
Ruy P de C, Barros II, Rosa RCA, Plaça JR, Corveloni AC, Cardoso C, Souza AF de, Biagi Junior CAO de, Siena ÁDD, Zueli KP, Tellechea MF, Carvalho S da C e S, Molfetta GA de, Pina Neto JM de, Silva Junior WA da. Analysis of potential disease-causing variants in a patient with intellectual disability via whole-exome sequencing [Internet]. Proceedings. 2019 ;[citado 2024 abr. 18 ] Available from: http://drive.ab3c.org.br/index.php/s/WDdbkSCMs5onm49 -
Vancouver
Ruy P de C, Barros II, Rosa RCA, Plaça JR, Corveloni AC, Cardoso C, Souza AF de, Biagi Junior CAO de, Siena ÁDD, Zueli KP, Tellechea MF, Carvalho S da C e S, Molfetta GA de, Pina Neto JM de, Silva Junior WA da. Analysis of potential disease-causing variants in a patient with intellectual disability via whole-exome sequencing [Internet]. Proceedings. 2019 ;[citado 2024 abr. 18 ] Available from: http://drive.ab3c.org.br/index.php/s/WDdbkSCMs5onm49 - The loss of a long noncoding RNA can lead to delayed neural development
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