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Q35195883-1FBDF8E7-DA65-4E2D-95B8-30B6C6264EEB
Q35195883-1FBDF8E7-DA65-4E2D-95B8-30B6C6264EEB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35195883-1FBDF8E7-DA65-4E2D-95B8-30B6C6264EEB
Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q.
P2860
Q35195883-1FBDF8E7-DA65-4E2D-95B8-30B6C6264EEB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35195883-1FBDF8E7-DA65-4E2D-95B8-30B6C6264EEB
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Statement
wasDerivedFrom
cb2864f40df5bbb9da9a1f55c53906b619a411a3
P2860
WAARDENBURG'S SYNDROME AND HETEROCHROMIA IRIDUM IN A DEAF SCHOOL POPULATION