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Q24670212-A498C57E-775F-4E9B-B680-13FD39A6B5C5
Q24670212-A498C57E-775F-4E9B-B680-13FD39A6B5C5
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Statement
http://www.wikidata.org/entity/statement/Q24670212-A498C57E-775F-4E9B-B680-13FD39A6B5C5
Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium
P2860
Q24670212-A498C57E-775F-4E9B-B680-13FD39A6B5C5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24670212-A498C57E-775F-4E9B-B680-13FD39A6B5C5
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wasDerivedFrom
767dd6292991b86f47315ed82cfcec2e5531dd16
P2860
Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q.