Showing 37–45 of 76 results
-
HECT E3s and human disease
-
Human chromosome 21 gene expression atlas in the mouse
-
Impairment in the cognitive functioning of men with fragile X-associated tremor/ataxia syndrome (FXTAS)
-
Investigation of the molecular mechanisms underlying Down syndrome phenotypes
-
L’épilepsie dans le syndrome de l’X fragile
-
La personne handicapée mentale et la société
-
Methylation profiling in individuals with uniparental disomy identifies novel differentially methylated regions on chromosome 15
-
Mouse models for Down Syndrome-Associated Developmental Cognitive Disabilities
-
Nineteen Additional Unpredicted Transcripts from Human Chromosome 21