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Q42586197-72691800-3781-4879-9440-72FA60E9A68C
Q42586197-72691800-3781-4879-9440-72FA60E9A68C
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Statement
http://www.wikidata.org/entity/statement/Q42586197-72691800-3781-4879-9440-72FA60E9A68C
Disruption of PCP signaling causes limb morphogenesis and skeletal defects and may underlie Robinow syndrome and brachydactyly type B.
P2860
Q42586197-72691800-3781-4879-9440-72FA60E9A68C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42586197-72691800-3781-4879-9440-72FA60E9A68C
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wasDerivedFrom
f913f3b0ce93cc5613ed1c641e05e400284c461a
P2860
One gene, two phenotypes: ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B.