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Identification of rare copy number polymorphic gains at 3q12.2 and 19q13.2 identifies candidate genes for familial endometriosis

ABSTRACT: The association between endometriosis, genomic copy number variant polymorphisms and differential gene expression is still unclear. The rationale of this study was to identify regions of copy number change in familial endometriosis, which could contain genes that may be involved with the susceptibility and progression of this disease.

ORGANISM(S): Homo sapiens

PROVIDER: GSE85701 | GEO | 2016/08/17

SECONDARY ACCESSION(S): PRJNA339134

REPOSITORIES: GEO

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