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Article

Comparison of microarray‐based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens

22 Jul 2008

Abstract excerpt

OBJECTIVE: To compare the detection rate by microarray analysis for chromosome abnormalities in a prenatal population to that of a neonatal population referred for diagnostic testing. METHODS: Array comparative genomic hybridization (aCGH) analysis was performed for 151 prenatal cases and compared with the results from 1375 postnatal cases less than 3 months of age. RESULTS: Two of 151 prenatal cases (1.3%)...

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Share to Genomic variations and chromosomal abnormalities
Share to Genomics and Rare Diseases
Share to Prenatal Screening and Diagnostics

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PMID: 18646242
DOI: 10.1002/pd.2053

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