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Details
Link-It Detail - PubMed - "Mowat-Wilson" syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene.
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PubMed (1)
"Mowat-Wilson" syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene. 11891681
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanZEB29839zinc finger E-box binding homeobox 2
PUBMED, Pubmed Id: 11891681, PUBMED ID: 11891681
XRefs (1)

XRef Types:
pubmed : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
PUBMEDimg 11891681"Mowat-Wilson" syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene.0self