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Vialard F et al. - Chromosomal imbalances were therefore detected and/or characterized in 6 of 39 fetuses, indicating the value of routine array CGH in cases of MCAs and in uncharacterized chromosome rearrangements. Extension to all prenatal diagnoses may be warranted when copy number variation is identified and all FISH probes are commercially available.

Today in Perinatal...keeping you current

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