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Raoul Hennekam

PROF.DR.

Medical Specialist, APH - Quality of Care

Research activity per year

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23 Article
3 Review article
1 Chapter
1 Comment/Letter to the editor
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- 1 Letter

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Dihydropyrimidine dehydrogenase deficiency: Homozygosity for an extremely rare variant in DPYD due to uniparental isodisomy of chromosome 1
van Kuilenburg, A. B. P., Meijer, J., Meinsma, R., Pérez-Dueñas, B., Alders, M., Bhuiyan, Z. A., Artuch, R. & Hennekam, R. C. M., 1 Jan 2019, JIMD Reports. Springer, Vol. 45. p. 65-69 (JIMD Reports).
Research output: Chapter in Book/Report/Conference proceeding › Chapter › Academic › peer-review