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pro vyhledávání: '"Eduarda Morgana da Silva Montenegro"'
Akademický článek
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Autor:
Silvia S. Costa, Naila Cristina Vilaça Lourenço, Eloisa de Sá Moreira, Isabela Maya Wahys Silva, Ana Cristina Victorino Krepischi, Elaine Cristina Zachi, Angela Maria Vianna-Morgante, Eduarda Morgana da Silva Montenegro, Mehdi Zarrei, Claudia Ismania Samogy Costa, Elisa Varella Branco, Maria Rita Passos-Bueno, Stephen W. Scherer, Jaqueline Yu Ting Wang, Marilia O. Scliar, Carla Rosenberg
Publikováno v:
Clinical Genetics. 101:134-141
Prediction of pathogenicity of rare copy number variations (CNVs), a genomic alteration known to contribute to the etiology of autism spectrum disorder (ASD), represents a serious limitation to interpreting genetic tests, particularly for genetic cou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25d87ce292ebeec4d95e37f3851e9f64
https://doi.org/10.1111/cge.14072
https://doi.org/10.1111/cge.14072
Autor:
Claudia Ismania Samogy Costa, Elisa Varella Branco, Ana Cristina Victorino Krepischi, Stephen W. Scherer, Silvia S. Costa, Maria Rita Passos-Bueno, Mehdi Zarrei, Jaqueline Yu Ting Wang, Angela Maria Vianna-Morgante, Marilia O. Scliar, Isabela Maya Wahys Silva, Carla Rosenberg, Naila Cristina Vilaça Lourenço, Elaine Cristina Zachi, Eduarda Morgana da Silva Montenegro, Eloisa de Sá Moreira
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6ec641422d310e6cefef5bcbffe037d
https://doi.org/10.1111/cge.14072/v2/response1
https://doi.org/10.1111/cge.14072/v2/response1
Autor:
Elaine Cristina Zachi, Tatiana F. Almeida, Guilherme L. Yamamoto, Gabriele Campos, Mehdi Zarrei, Ada J.S. Chan, Eduarda Morgana da Silva Montenegro, Marilia O. Scliar, Isabela Maya Wahys Silva, Maria Rita Passos-Bueno, Claudia Ismania Samogy Costa, Stephen W. Scherer, Naila Cristina Vilaça Lourenço
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Large genomic databases of neurodevelopmental disorders (NDD) are helpful resources of genomic variations in complex and heterogeneous conditions, as Autism Spectrum Disorder (ASD). We evaluated the role of rare copy number variations (CNVs) and exon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d672c9934d3b4ab754313c0cbcdac61e
https://doi.org/10.1002/aur.2238
https://doi.org/10.1002/aur.2238
Autor:
Eduarda Morgana da Silva Montenegro, André Oliveira de Souza Lima, Gabriela Scholante Delabary, Fernando Dini Andreote, Marcus Adonai Castro da Silva
Publikováno v:
Bioengineering; Volume 4; Issue 2; Pages: 52
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Bioengineering
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Bioengineering
The use of molecular diagnostic techniques for bioprospecting and microbial diversity study purposes has gained more attention thanks to their functionality, low cost and quick results. In this context, ten degenerate primers were designed for the am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61df2246161bc86ae48466573db07edd