Robin de Putter
- ORCID iD
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0000-0001-9410-8941
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Multiple European children born with cancer predisposition following recurrent sperm donation from a mosaic TP53 carrier
(2025) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 33(Supplement 1). p.37-37 -
- Journal Article
- A1
- open access
The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS)
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- Journal Article
- A1
- open access
Wilms tumor characteristics in children with heterozygous germline DIS3L2 variants
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- Journal Article
- A2
- open access
Cancer prognosis and treatment results in patients with PTEN Hamartoma Tumour Syndrome (PHTS) : a European cohort study
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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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Harnessing cDNA analysis to enhance variant classification in cancer predisposition genes
(2024) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 32(Supplement 2). p.1273-1273 -
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