A Patient With a Mild Holoprosencephaly Spectrum Phenotype and Heterotaxy and a 1.3 Mb Deletion Encompassing GLI2

Sietske H. G. Kevelam*, Jeske J. T. van Harssel, Bert van der Zwaag, Hubertus J. M. Smeets, Aimee D. C. Paulussen, Klaske D. Lichtenbelt

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)166-173
JournalAmerican Journal of Medical Genetics Part A
Issue number1
Publication statusPublished - Jan 2012


  • GLI2
  • array comparative genomic hybridization
  • deletion
  • holoprosencephaly
  • heterotaxy

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