Showing 19–27 of 76 results
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Débilité mentale et trouble du comportement
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Déficience intellectuelle et psychopathologie: instruments d’évaluation et application dans l’étude du phénotype comportemental des adultes avec syndrome de Down
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Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype
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Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations
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Deviant trajectories of cortical maturation in 22q11.2 deletion syndrome (22q11DS): A cross-sectional and longitudinal study
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DNA-Methylation Patterns in Trisomy 21 Using Cells from Monozygotic Twins
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Domains of genome-wide gene expression dysregulation in Down’s syndrome
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Effect of Obesity Onset on Pendular Energy Transduction at Spontaneous Walking Speed: Prader–Willi Versus Nonsyndromal Obese Individuals
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Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes