Research interests

genome diagnostics i.p. epigenetics of disease

PubMed database           Mannens M M A M, Mannens H M A M, Mannens M, Mannens M A, Mannens M A M, Mannens M M, Mannens M A M M, Mannens M M A

specialisation

Genome diagnostics i.p. epigenetics of disease

Research output

  1. Mutations in CCBE1 cause generalized lymph vessel dysplasia in humans

    Research output: Contribution to journal › Article › Academic › peer-review

  2. Mutations in ZBTB20 cause Primrose syndrome

    Research output: Contribution to journal › Article › Academic › peer-review

  3. Yield of molecular and clinical testing for arrhythmia syndromes: report of 15 years' experience

    Research output: Contribution to journal › Article › Academic › peer-review

  4. Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic features

    Research output: Contribution to journal › Article › Academic › peer-review

  5. Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype

    Research output: Contribution to journal › Article › Academic › peer-review

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Projects

  1. Mannens M.M.A.M.: Clinical Molecular Genetics with emphasis on cardiogenetics and growth malformations

    Project: Research

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