Unknown,Transcriptomics,Genomics,Proteomics

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Oligo array for CNV calling AUTS2 project [Agilent]

ABSTRACT: Phenotypic and genotypic description of AUTS2 deletion patients found by Array analysis in an international cohort of intellectual disability (ID) and multiple congenital malformations (MCA). Arrays were hybridized and analysed using manufacturer's protocols on DNA from patients with ID/MCA

ORGANISM(S): Homo sapiens

SUBMITTER: Els Voorhoeve 

PROVIDER: E-GEOD-37141 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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