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Interstitial deletion and ring chromosome derived from 16q.
  1. C M Krauss,
  2. D Caldwell,
  3. L Atkins

    Abstract

    An interstitial deletion of 16q was identified in an infant with failure to thrive, dysmorphic facies, and congenital heart defects. The mother of this infant had a similar deletion of 16q with ring formation of a fragment presumed to be derived from the deleted portion of 16q. We discuss these cases and compare them to other reports of 16q deletions.

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