A patient with a mild holoprosencephaly spectrum phenotype and heterotaxy and a 1.3 Mb deletion encompassing GLI2

Translated title of the contribution: A patient with a mild holoprosencephaly spectrum phenotype and heterotaxy and a 1.3 Mb deletion encompassing GLI2

S.H. Kevelam, J.J.T. van Harssel, A. van der Zwaag, H.J.M. Smeets, A.D.C. Paulussen, K.D. Lichtenbelt

Research output: Contribution to journalArticleAcademicpeer-review

Translated title of the contributionA patient with a mild holoprosencephaly spectrum phenotype and heterotaxy and a 1.3 Mb deletion encompassing GLI2
Original languageUndefined/Unknown
Pages (from-to)166-173
Number of pages8
JournalAmerican Journal of Medical Genetics. Part A
Volume158A
Issue number1
DOIs
Publication statusPublished - 2012

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