Oligo array for CNV calling AUTS2 project [Agilent]
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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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