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Q24514967-F2FBCD74-C20B-4F2E-81E1-8551912C1D5D
Q24514967-F2FBCD74-C20B-4F2E-81E1-8551912C1D5D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24514967-F2FBCD74-C20B-4F2E-81E1-8551912C1D5D
Splotch locus mouse mutants: models for neural tube defects and Waardenburg syndrome type I in humans.
P2860
Q24514967-F2FBCD74-C20B-4F2E-81E1-8551912C1D5D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24514967-F2FBCD74-C20B-4F2E-81E1-8551912C1D5D
rank
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type
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Statement
wasDerivedFrom
a4da5fd9006ef9fb35b7530997415a004fc28107
P2860
Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q.