From Karyotyping to Array-CGH in Prenatal Diagnosis

Abstract excerpt

Conventional karyotyping detects chromosomal anomalies in up to 35% of pregnancies with fetal ultrasound anomalies, depending on the number and type of these anomalies. Extensive experience gained in the past decades has shown that prenatal karyotyping is a robust technique which can detect the majority of germline chromosomal anomalies. For most of these anomalies the phenotype is known. In postnatal diagnosis...

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• Share to Fetal and Pediatric Neurological Disorders
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