CNVs in spermatogenic failure

ABSTRACT: To determine the involvement of Copy Number Variants (CNVs) in the origin of male infertility, patients with idiopathic severe oligozoospermia, Sertoli-cell-only syndrome and controls with normozoospermia were analysed by array CGH using the 244A/400K array sets (Agilent Technologies).

ORGANISM(S): Homo sapiens

PROVIDER: GSE27965 | GEO | 2011/03/17

SECONDARY ACCESSION(S): PRJNA137757

REPOSITORIES: GEO