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16q24.1 microdeletion in a premature newborn: usefulness of array-based comparative genomic hybridation (array CGH) in persistent pulmonary hypertension of the newborn
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A measurement of the ratio of the W and Z cross sections with exactly one associated jet in pp collisions at √es=7 TeV with ATLAS
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A propos d’emplois ouverts à des handicapés dans quelques entreprises et une administration du canton de Vaud
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A t(7;12) Balanced Translocation With Breakpoints Overlapping Those of the Williams–Beuren and 12q14 Microdeletion Syndromes
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Allocentric spatial learning and memory deficits in Down syndrome
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An atypical 7q11.23 deletion in a normal IQ Williams–Beuren syndrome patient
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Another cause of vaccine encephalopathy: A case of Angelman syndrome
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Association between Foot Growth and Musculoskeletal Loading in Children with Prader-Willi Syndrome before and during Growth Hormone Treatment
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Brief Report: Isogenic Induced Pluripotent Stem Cell Lines From an Adult With Mosaic Down Syndrome Model Accelerated Neuronal Ageing and Neurodegeneration
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Carriers of the fragile X mental retardation 1 (FMR1) premutation allele present with increased levels of cytokine IL-10
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Classification of Functioning and Impairment: The Development of ICF Core Sets for Autism Spectrum Disorder
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Cognition and Hippocampal Plasticity in the Mouse Is Altered by Monosomy of a Genomic Region Implicated in Down Syndrome
