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Q33680415-9B28B0EA-F97A-48E5-88A1-6C32B18E1374
Q33680415-9B28B0EA-F97A-48E5-88A1-6C32B18E1374
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33680415-9B28B0EA-F97A-48E5-88A1-6C32B18E1374
Septo-optic dysplasia and WS1 in the proband of a WS1 family segregating for a novel mutation in PAX3 exon 7.
P2860
Q33680415-9B28B0EA-F97A-48E5-88A1-6C32B18E1374
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33680415-9B28B0EA-F97A-48E5-88A1-6C32B18E1374
rank
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type
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Statement
wasDerivedFrom
ed983bf44df4e4cad4af6058ae24016592170515
P2860
Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q.