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Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies
Objective To demonstrate the usefulness of microarray testing in prenatal diagnosis based on our laboratory experience. Methods Prenatal samples received from 2004 to 2011 for a variety ofExpand
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Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound
Objective The aim of this study is to understand the diagnostic utility of comparative genomic hybridization (CGH)-based microarrays for pregnancies with abnormal ultrasound findings. Methods WeExpand
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Investigation of NRXN1 deletions: Clinical and molecular characterization
Deletions at 2p16.3 involving exons of NRXN1 are associated with susceptibility for autism and schizophrenia, and similar deletions have been identified in individuals with developmental delay andExpand
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Referral patterns for microarray testing in prenatal diagnosis.
OBJECTIVE To understand the prenatal referral patterns from the United States, Canada, and Israel for two whole-genome microarray platforms, each with a different resolution. METHOD PhysiciansExpand
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Referral patterns for microarray testing in prenatal diagnosis.
Objective To understand the prenatal referral patterns from the United States, Canada, and Israel for two whole-genome microarray platforms, each with a different resolution. Method PhysiciansExpand
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Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysis
Purpose:To understand the ability of microarray-based comparative genomic hybridization to detect copy-number variation in the presence of maternal cell contamination.Methods:To simulate maternalExpand
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