PRJNA558095 - Predictive impact of rare genomic copy number variations in high-risk infant siblings of individuals with autism - OmicsDI

Genomics

Dataset Information

Predictive impact of rare genomic copy number variations in high-risk infant siblings of individuals with autism

ABSTRACT: Predictive impact of rare genomic copy number variations in high-risk infant siblings of individuals with autism

PROVIDER: PRJNA558095 | ENA |

REPOSITORIES: ENA