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

S.H.G. Kevelam, J.J. van Harssel, B. van der Zwaag, H.J. Smeets, A.D. Paulussen, K.D. Lichtenbelt

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)166-173
JournalAmerican Journal of Medical Genetics Part A
Volume158A
Issue number1
DOIs
Publication statusPublished - 2012

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