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 journalArticleAcademicpeer-review

  2. Mutations in ZBTB20 cause Primrose syndrome

    Research output: Contribution to journalArticleAcademicpeer-review

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

    Research output: Contribution to journalArticleAcademicpeer-review

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

    Research output: Contribution to journalArticleAcademicpeer-review

View all (200) »

ID: 72026