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Q47155566-A8EB8C4D-8861-4163-8039-5DA83F7F9333
Q47155566-A8EB8C4D-8861-4163-8039-5DA83F7F9333
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http://www.wikidata.org/entity/statement/Q47155566-A8EB8C4D-8861-4163-8039-5DA83F7F9333
Involvement of the bone morphogenic protein/SMAD signaling pathway in the etiology of congenital anomalies of the kidney and urinary tract accompanied by cryptorchidism.
P2860
Q47155566-A8EB8C4D-8861-4163-8039-5DA83F7F9333
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47155566-A8EB8C4D-8861-4163-8039-5DA83F7F9333
rank
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wasDerivedFrom
cf333936b69d865d23b862bbba0e95c58c16cb0d
P2860
Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract.