The frequency of CNVs in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancy
ConclusionOur systematic approach of ascertaining congenital anomalies resulted in explaining the etiology of congenital anomalies in 47% of fetuses after the termination of pregnancy. By using array comparative genomic hybridization, we found that copy number variations represent an important part in the etiology of multiple, as well as isolated congenital anomalies, which indicates the importance of analyzing copy number variations in the diagnostic approach of fetuses with congenital anomalies after the termination of pregnancy.
Source: Molecular Genetics & Genomic Medicine - Category: Genetics & Stem Cells Authors: Gorazd Rudolf,
Luca Lovre čić,
Nataša Tul,
Nataša Teran,
Borut Peterlin Tags: ORIGINAL ARTICLE Source Type: research