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Jul
Mowat-Wilson syndrome chromosome 2 deletions
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Mowat-Wilson syndrome and chromosome 2 deletions Mowat-Wilson syndrome (MWS) caused by mutations of the ZEB2 gene (or deletions of 2q22 chromosomal segment where this gene is located) is characterized by microcephaly, distinctive facial features, Hirschsprung disease, developmental delay, some other congenital anomalies, epilepsy, and behavioral problems. Recent publications by Liang... Read More
