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A case of interstitial deletion of 10q25.2----q26.1.
  1. D E Rooney,
  2. K Williams,
  3. D V Coleman,
  4. A Habel
  1. Cytogenetics Unit, St Mary's Hospital, London.

    Abstract

    A de novo interstitial deletion of chromosome 10, del(10)(pter----q25.2::q26.1----qter), was detected in a newborn female with facial anomalies, failure to thrive, and subsequent developmental delay. This case is compared with 10 previous reports of monosomy 10q within the q25----qter region.

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