Associated Papers
Expanding the Genetic and Phenotypic Spectrum of Mowat-Wilson Syndrome: A Study of 10 Turkish Patients With an Intrafamilial Recurrence Caused by First Intragenic Large Deletion.
Kablan A et al.
American Journal of Medical Genetics. Part A, 2025
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
PEDIA: prioritization of exome data by image analysis.
Hsieh TC et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019
31164752 (PubMed )
Supplement: 41436_2019_566_MOESM2_ESM.xlsx › Sheet1
Clinical spectrum of eye malformations in four patients with Mowat-Wilson syndrome.
Bourchany A et al.
American Journal of Medical Genetics. Part A, 2015
Ocular phenotype of Mowat-Wilson syndrome in the first reported Cypriot patients: an under-recognized association.
Tanteles GA et al.
Clinical Dysmorphology, 2014
ZFHX1B mutations in patients with Mowat-Wilson syndrome.
Dastot-Le Moal F et al.
Human Mutation, 2007
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