Genomics

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Oligo array for calling CNV's for AUTS2 project [NimbleGen]

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).

ORGANISM(S): Homo sapiens

PROVIDER: GSE37654 | GEO | 2012/07/12

SECONDARY ACCESSION(S): PRJNA170383

REPOSITORIES: GEO

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