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Developmental disability and hypomelanosis of Ito in a female with 7.3 Mb de novo duplication of Xp11.3-p11.4 and random X inactivation

Research output: Contribution to journalLetterpeer-review

Original languageEnglish (US)
Pages (from-to)2573-2577
Number of pages5
JournalAmerican Journal of Medical Genetics, Part A
Volume149
Issue number11
DOIs
StatePublished - Nov 2009
Externally publishedYes

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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