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Q54952133-301A631E-EAEB-4368-B9B9-138D00CBB020
Q54952133-301A631E-EAEB-4368-B9B9-138D00CBB020
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54952133-301A631E-EAEB-4368-B9B9-138D00CBB020
Sensorineural deafness, distinctive facial features, and abnormal cranial bones: a new variant of Waardenburg syndrome?
P2860
Q54952133-301A631E-EAEB-4368-B9B9-138D00CBB020
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54952133-301A631E-EAEB-4368-B9B9-138D00CBB020
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wasDerivedFrom
bb18664e556dbdd3ef4bdfdfa34698622e3821ef
P2860
Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I)