bcor-regulated-genes-in-human-oculo-facio-cardio-d02apicaleyegenetic disordersyndromehumanFalseE-GEOD-152143211BCOR-regulated genes in human oculo-facio-cardio-dental syndromeglobal-gene-expression-profiles-of-ipsc-from-sma-p29diseasegenetic disordermotor neuronmotor neuron diseasemuscular atrophyneuronspinal muscular atrophyhumanFalseE-GEOD-272062593Global gene expression profiles of iPSC from SMA patient, unaffected father and iPS 19.9 compared to transcriptomic data obtained by corresponding fibroblaststranscription-profiling-of-primary-fibroblasts-fro19genetic disordergenomehutchinson-gilford progeria syndromelamin anuclear laminaskinsyndromehumanFalseE-MEXP-30975175Transcription profiling of primary fibroblasts from a family with autosomal recessive Hutchinson-Gilford Progeria Syndromedifferential-gene-expression-and-mitochondrial-dys214brainchromosomegenetic disordergenomehearthypogonadismlivermorbid obesitymuscleobesityprader-willi syndromesyndromevastus lateralismouseFalseE-GEOD-417597051Differential Gene Expression and Mitochondrial Dysfunction in Imprinting center deletion (PWS- IC del) Mouse model of Prader-Willi Syndromegene-expression-analysis-of-spinal-cord-obtained-f212diseasegenetic disordermotor neuronmotor neuron diseasemuscular atrophyneuronspinal cordspinal muscular atrophymouseFalseE-GEOD-196748455Gene Expression Analysis of spinal cord obtained from a mouse model of severe Spinal Muscular Atrophy (SMA)