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- W2201383424 endingPage "120" @default.
- W2201383424 startingPage "112" @default.
- W2201383424 abstract "Congenital cardiovascular malformations (CVM) are among the most common of all medically significant birth defects. Yet, the cause of these malformations is unknown in the majority of cases. In live-born infants, chromosomal abnormalities detected by conventional karyotyping account for approximately one tenth of all cardiac malformations. In addition, genomic disorders often resulting from instability of the regional genomic architecture, constitute a major fraction of CVM. These events are usually submicroscopic, and are observed as genomic deletions and/or duplications. The widespread use of array-comparative genomic hybridization has uncovered numerous DNA copy number variations, often encompassing important dosage-sensitive genes that are functionally relevant for CVM." @default.
- W2201383424 created "2016-06-24" @default.
- W2201383424 creator A5033405102 @default.
- W2201383424 date "2015-01-01" @default.
- W2201383424 modified "2023-09-26" @default.
- W2201383424 title "Other Genomic Disorders Causing Congenital Cardiovascular Malformations" @default.
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