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Q36515048-62CF73E5-64D0-49B2-A0C1-5AE569E02B92
Q36515048-62CF73E5-64D0-49B2-A0C1-5AE569E02B92
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36515048-62CF73E5-64D0-49B2-A0C1-5AE569E02B92
Molecular etiology of arthrogryposis in multiple families of mostly Turkish origin.
P2860
Q36515048-62CF73E5-64D0-49B2-A0C1-5AE569E02B92
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36515048-62CF73E5-64D0-49B2-A0C1-5AE569E02B92
rank
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Statement
wasDerivedFrom
4f261580ae8f32ed3567ffb65c746a4a79aaafa2
P2860
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.