De novo duplication of chromosome 13(q32-q34) in a child with developmental delay

Research output: Contribution to journalArticle


We report the case of a child affected by a duplication of chromosome 13(q32-q34). This cytogenetic abnormality is rarely described in the literature. The description of our patient's characteristics might contribute to a better phenotype definition.

Original languageEnglish
Pages (from-to)1084-1085
Number of pages2
JournalJournal of Child Neurology
Issue number12
Publication statusPublished - Dec 2006


ASJC Scopus subject areas

  • Clinical Neurology
  • Pediatrics, Perinatology, and Child Health

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