Handicap Mental
Affichage de 19–27 sur 57 résultats
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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
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FMR1 CGG repeat length predicts motor dysfunction in premutation carriers
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Fragile X Premutation Tremor/Ataxia Syndrome: Molecular, Clinical, and Neuroimaging Correlates
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Fragile-X syndrome and fragile X-associated tremor/ataxia syndrome: two faces of FMR1