Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature

Merel Klaassens, Deborah Morrogh, Elisabeth M. Rosser, Fatima Jaffer, Maaike Vreeburg, Levinus A. Bok, Tim Segboer, Martine van Belzen, Ros M. Quinlivan, Ajith Kumar, Jane A. Hurst, Richard H. Scott

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)610-615
JournalEuropean Journal of Human Genetics
Volume23
Issue number5
DOIs
Publication statusPublished - May 2015

Cite this

Klaassens, M., Morrogh, D., Rosser, E. M., Jaffer, F., Vreeburg, M., Bok, L. A., Segboer, T., van Belzen, M., Quinlivan, R. M., Kumar, A., Hurst, J. A., & Scott, R. H. (2015). Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature. European Journal of Human Genetics, 23(5), 610-615. https://doi.org/10.1038/ejhg.2014.162