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Concurrent de novo interstitial deletion of band 2p22 and reciprocal translocation (3;7)(p21;q22).
  1. G C Webb,
  2. C G Keith,
  3. N T Campbell
  1. Department of Genetics, Royal Children's Hospital, Melbourne, Australia.

    Abstract

    A child is described with a de novo interstitial deletion of band 2p22 and a reciprocal translocation (3;7)(p21;q22). The child has mild developmental delay, coloboma of the right eye, and Hirschsprung's disease. The clinical and cytogenetic findings are described.

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