GSM2384996[Accession] - GEO DataSets

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Items: 3

Select item 2000895941.

Integrated network analysis reveals genotype-phenotype correlations in Williams syndrome

(Submitter supplied) Williams Syndrome (WS) is a rare neurodevelopmental disorder caused by heterozygous deletions in a chromosome 7q11.23 region typically encompassing 26-28 genes. WS patients exhibit a wide spectrum of symptoms, including cardiovascular disease, intellectual disability, visuospatial deficits and hypersociability a behavioral profile that contrasts with autism spectrum disorder (ASD). However, the relationship between neuropsychiatric phenotypes and dysregulated gene networks caused by the 7q11.23 deletion is unknown. more...

Organism:: Homo sapiens

Type:: Expression profiling by array

Platform:: GPL16699
94 Samples

Download data: TXT

Series

Accession:: GSE89594

ID:: 200089594

PubMed Full text in PMC Similar studies Analyze with GEO2R

Select item 1000166992.

Agilent-039494 SurePrint G3 Human GE v2 8x60K Microarray 039381 (Feature Number version)

(Submitter supplied) SurePrint G3 Human GE v2 8x60K Microarray Design ID: 039494 Design Format: 8 x 60 K Control Grid: IS-62976-8-V2_60kby8_GX_EQC_201000210 Build Version: hg19:GRCh37:Feb2009 Arrays of this design have barcodes that begin with 16039494 or 2539494. Orientation: Features are numbered numbered Left-to-Right, Top-to-Bottom as scanned by an Agilent scanner (barcode on the left, DNA on the back surface, scanned through the glass), matching the FeatureNum output from Agilent's Feature Extraction software. more...