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Q37176226-EA3F671A-F093-46C0-988B-DC87EE840BBB
Q37176226-EA3F671A-F093-46C0-988B-DC87EE840BBB
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Statement
http://www.wikidata.org/entity/statement/Q37176226-EA3F671A-F093-46C0-988B-DC87EE840BBB
Molecular Etiology of Hereditary Single-Side Deafness: Its Association With Pigmentary Disorders and Waardenburg Syndrome.
P2860
Q37176226-EA3F671A-F093-46C0-988B-DC87EE840BBB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37176226-EA3F671A-F093-46C0-988B-DC87EE840BBB
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type
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Statement
wasDerivedFrom
5bcb76efa09aa4e20dc1e3ba63743db30353d267
P2860
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations.