Jet Bliek
0000-0003-4549-6655
10 papers found
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Prevalence of (Epi)genetic Predisposing Factors in a 5-Year Unselected National Wilms Tumor Cohort: A Comprehensive Clinical and Genomic Characterization
Methylation analysis in tongue tissue of BWS patients identifies the (EPI)genetic cause in 3 patients with normal methylation levels in blood
Monozygotic twins discordant for vascular malformations and dysregulated growth
Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith–Wiedemann syndrome
Determination of KCNQ1OT1 and H19 methylation levels in BWS and SRS patients using methylation-sensitive high-resolution melting analysis
Epigenotype, Phenotype, and Tumors in Patients with Isolated Hemihyperplasia
Hypomethylation of the H19 Gene Causes Not Only Silver-Russell Syndrome (SRS) but Also Isolated Asymmetry or an SRS-Like Phenotype
Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome
Epigenotyping as a tool for the prediction of tumor risk and tumor type in patients with Beckwith-Wiedemann syndrome (BWS)
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