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Q34162216-4E0412B0-7C5D-4B58-9534-918B1EA98BD4
Q34162216-4E0412B0-7C5D-4B58-9534-918B1EA98BD4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34162216-4E0412B0-7C5D-4B58-9534-918B1EA98BD4
Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregate.
P2860
Q34162216-4E0412B0-7C5D-4B58-9534-918B1EA98BD4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34162216-4E0412B0-7C5D-4B58-9534-918B1EA98BD4
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Statement
wasDerivedFrom
2418a4b4e0626170d1013fc389390e3b72ac8099
P2860
A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1)