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Simultaneous de novo interstitial deletion of 16q21 and intercalary duplication of 19q in a retarded infant with minor dysmorphic features.
  1. U Trautmann,
  2. R A Pfeiffer,
  3. U Seufert-Satomi,
  4. H U Tietze
  1. Institut für Humangenetik, Friedrich-Alexander Universität Erlangen-Nürnberg, Germany.

    Abstract

    We report on a retarded infant with minor dysmorphic features in whom deletion 16 and duplication 19q were discovered. The karyotype is 46,XX,del(16) (q13.08-21.05),dup(19)(q13.13-13.2). The origin and significance of the aberrant chromosomes are unknown.

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