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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Kevelam, S. H. G., van Harssel, J. J., van der Zwaag, B., Smeets, H. J., Paulussen, A. D., & Lichtenbelt, K. D. (2012). A Patient With a Mild Holoprosencephaly Spectrum Phenotype and Heterotaxy and a 1.3 Mb Deletion Encompassing GLI2. American Journal of Medical Genetics Part A, 158A(1), 166-173. https://doi.org/10.1002/ajmg.a.34350