Genomic architecture of fetal central nervous system anomalies using whole-genome sequencing

Abstract excerpt

Structural anomalies of the central nervous system (CNS) are one of the most common fetal anomalies found during prenatal imaging. However, the genomic architecture of prenatal imaging phenotypes has not yet been systematically studied in a large cohort. Patients diagnosed with fetal CNS anomalies were identified from medical records and images. Fetal samples were subjected to low-pass and deep whole-genome...

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• Share to Fetal and Pediatric Neurological Disorders
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