75 research outputs found
Complementary feeding patterns in the first year of life in the city of Rio de Janeiro, Brazil: time trends from 1998 to 2008
Utilizando técnicas de ensino participativas como instrumento de aprendizagem e sensibilização do manejo da lactação para profissionais de enfermagem de uma maternidade
Copy number variants prioritization after array-CGH analysis - a cohort of 1000 patients
Array-based comparative genomic hybridization has been assumed to be the first genetic test offered to detect genomic imbalances in patients with unexplained intellectual disability with or without dysmorphisms, multiple congenital anomalies, learning difficulties and autism spectrum disorders. Our study contributes to the genotype/phenotype correlation with the delineation of laboratory criteria which help to classify the different copy number variants (CNVs) detected. We clustered our findings into five classes ranging from an imbalance detected in a microdeletion/duplication syndrome region (class I) to imbalances that had previously been reported in normal subjects in the Database of Genomic Variants (DGV) and thus considered common variants (class IV).info:eu-repo/semantics/publishedVersio
Exclusive breastfeeding duration and determinants among Brazilian children under two years of age
Cobertura populacional do Sistema de Vigilância Alimentar e Nutricional no Estado de São Paulo, Brasil
Factors associated with exclusive breastfeeding in the Legal Amazon and Northeast regions, Brazil, 2010
Associação entre o grau de implantação da Rede Amamenta Brasil e indicadores de amamentação
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