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Terminal deletion of the long arm of chromosome 10.
  1. H Curtis,
  2. R T Howell,
  3. C Cope

    Abstract

    A de novo chromosome abnormality interpreted as a terminal deletion of chromosome 10, del(10)(pter----q25.2:), was ascertained in a newborn female with multiple malformations. The clinical features observed at birth and on follow up at 10 months of age are described and compared with previously reported cases.

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