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#613266 - WAARDENBURG SYNDROME, TYPE 4C; WS4C
Cytogenetic locations: 147240
Gene summaries Genetic tests Medical literature
#611584 - WAARDENBURG SYNDROME, TYPE 2E; WS2E
#609136 - PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH
*602229 - SRY-BOX 10; SOX10
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