Prenatal diagnosis of congenital heart defect by genome-wide high-resolution SNP array
Prenatal Diagnosis2014Vol. 34(9), pp. 858–863
Citations Over TimeTop 11% of 2014 papers
Abstract
Our results demonstrated the value of high-resolution SNP arrays in prenatal diagnosis of CHD; it should become an integral aspect in clinically molecular diagnosis and genetic counseling. The complexity of the cardiac defect was not related to the frequency of clinical significant CNV, but the presence of neurologic defect was related.
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