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Large deletion in PIGL: a common mutational mechanism in CHIME syndrome?
Bertola, Debora R.
Date: 2018
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Origin: Oasisbr
Detection of small copy number variations (CNVs) in autism spectrum disorder (A...
Moreira, Eloisa S.; Silva, Isabela M. W.; Lourenco, Naila; Moreira, Danielle P.; Ribeiro, Cintia M.; Martins, Ana Luiza B. [UNESP]Made available in DSpace on 2018-11-26T17:55:47Z (GMT). No. of bitstreams: 0 Previous issue date: 2016-03-01; Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP); Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq); Autism spectrum disorder (ASD) has a strong genetic basis and advances in genomic scanning methods have resulted in the identification of the underlying alterations in abo...
Date: 2018
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Origin: Oasisbr
Autoimmune disease and multiple autoantibodies is 42 patients with RASopathies
Bertola, Debora R.
Date: 2012
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Origin: Oasisbr