Associated Papers
Identification of the DNA methylation signature of Mowat-Wilson syndrome.
Caraffi SG et al.
European Journal of Human Genetics : Ejhg, 2024
38351292 (PubMed )
Supplement: 41431_2024_1548_MOESM1_ESM.pdf
Three Novel De Novo ZEB2 Variants Identified in Three Unrelated Chinese Patients With Mowat-Wilson Syndrome and A Systematic Review.
Fu Y et al.
Frontiers in Genetics, 2022
35646055 (PubMed )
Supplement: DataSheet1.xls › All_the_ZEB2_variants
Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care.
Ivanovski I et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2018
CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases.
Wenger TL et al.
American Journal of Medical Genetics. Part A, 2014
Epilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotype.
Cordelli DM et al.
American Journal of Medical Genetics. Part A, 2013
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