J. Vliet

Increased DNA methylation at the AXIN1 gene in a monozygotic twin from a pair discordant for a caudal duplication anomaly.

D. Duffy, N. Martin, D. Boomsma, 2006, American journal of human genetics.

Myotonic dystrophy type 2. The challenging diagnosis of a complex disease

J. V. Vliet, J. Vliet, 2019 .

No relevant excess prevalence of myotonic dystrophy type 2 in patients with suspected fibromyalgia syndrome

B. Engelen, H. Scheffer, A. Tieleman, 2016, Neuromuscular Disorders.

Epigenetic mechanisms in the context of complex diseases

E. Whitelaw, J. V. Vliet, N. Oates, 2007, Cellular and Molecular Life Sciences.

EEG Leading to the Diagnosis of Limbic Encephalitis

J. Meulstee, W. Mulleners, Judith van Vliet, 2012, Clinical EEG and neuroscience.