Robin de Putter
- ORCID iD
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0000-0001-9410-8941
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- Journal Article
- A1
- open access
Cracking rare disorders : a new minimally invasive RNA-seq protocol
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- Journal Article
- A1
- open access
Family-level impact of germline genetic testing in childhood cancer : a multi family member interview analysis
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Clinical impact of RNA-sequencing in diagnostics
(2024) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 32(Supplement 1). p.648-648 -
- Journal Article
- A1
- open access
Lifestyle factors and breast cancer in females with PTEN Hamartoma Tumor Syndrome (PHTS)
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Cancer prognosis in PTEN Hamartoma Tumor Syndrome : a European cohort study
(2024) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 32(Supplement 1). p.563-564 -
- Journal Article
- A1
- open access
Genetic counselling legislation and practice in cancer in EU Member States
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- Journal Article
- A1
- open access
The heterogeneous cancer phenotype of individuals with biallelic germline pathogenic variants in CHEK2
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- Journal Article
- A1
- open access
The psychological impact of genetic testing in childhood cancer : a systematic review
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Biallelic pathogenic variants in CHEK2 predispose to multiple primary tumours
(2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.549-549 -
Clinical and Wilms tumor characteristics of patients with heterozygous germline DIS3L2 variants