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Q28590779-A3715CCA-FBE0-4AA3-A756-BBE99AA65CB3
Q28590779-A3715CCA-FBE0-4AA3-A756-BBE99AA65CB3
BestRank
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http://www.wikidata.org/entity/statement/Q28590779-A3715CCA-FBE0-4AA3-A756-BBE99AA65CB3
Ror2 knockout mouse as a model for the developmental pathology of autosomal recessive Robinow syndrome
P2860
Q28590779-A3715CCA-FBE0-4AA3-A756-BBE99AA65CB3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28590779-A3715CCA-FBE0-4AA3-A756-BBE99AA65CB3
rank
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type
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Statement
wasDerivedFrom
a68fc0434f5e31b5b7cd53df39c771b095090a90
P2860
Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B