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MYCN activation in hTERT immortalized RPE cells as model for oncogene induced senescence
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Criteria for reporting incidental findings in clinical whole exome sequencing : professional practice and perspective in Belgian genetic centres
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SOX11 is a key epigenetic regulator in the adrenergic MYCN amplified neuroblastoma
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The zebrafish as a model for recessive types of osteogenesis imperfecta
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Shallow whole genome sequencing on circulating cell-free DNA in pediatric cancer patients
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Heterozygous defects in collagen XII cause myopathic Ehlers-Danlos syndrome and lead to variant-specific alterations in the extracellular matrix
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Loss of galactosyltransferase II, encoded by B3GALT6, causes skeletal abnormalities in a zebrafish model for spondylodysplastic Ehlers-Danlos syndrome, the B3GALT6 type
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- Conference Paper
- C3
- open access
Expanding the genotypic and phenotypic spectrum of the B3GAT3 linkeropathy
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Application of a custom designed broad cancer predisposition gene panel for the analysis of patients with a personal and/or family history of pancreatic cancer
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Detection of genome-wide copy number alterations in tumor tissue and cell-free DNA of pancreatic cancer patients