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Copy number variants analysis of heterotaxy syndrome patients with congenital heart defects

ABSTRACT: To identify the molecular causes of heterotaxy syndrome patients with congenital heart defects, an Affymetrix CytoScan HD array was used to identify possible pathogenic CNVs in 63 patients. A total of 59 samples passed initial quality control.

ORGANISM(S): Homo sapiens

SUBMITTER: Xu Rang

PROVIDER: E-MTAB-6820 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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