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Q59128106-0ECB0EAA-C616-4F2A-9F4D-2C4A84B98421
Q59128106-0ECB0EAA-C616-4F2A-9F4D-2C4A84B98421
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http://www.wikidata.org/entity/statement/Q59128106-0ECB0EAA-C616-4F2A-9F4D-2C4A84B98421
Clinical Genetics of Polydactyly: An Updated Review
P2860
Q59128106-0ECB0EAA-C616-4F2A-9F4D-2C4A84B98421
BestRank
Statement
http://www.wikidata.org/entity/statement/Q59128106-0ECB0EAA-C616-4F2A-9F4D-2C4A84B98421
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wasDerivedFrom
1bae9e7990cd13999ae8c015e587cb46ef020689
P2860
Exome sequencing reveals a novel homozygous splice site variant in the WNT1 gene underlying osteogenesis imperfecta type 3.