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Q54163960-175C75B0-90C1-4574-8D2A-C7B46A86E3E8
Q54163960-175C75B0-90C1-4574-8D2A-C7B46A86E3E8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54163960-175C75B0-90C1-4574-8D2A-C7B46A86E3E8
Copy number variation as a genetic basis for heterotaxy and heterotaxy-spectrum congenital heart defects.
P2860
Q54163960-175C75B0-90C1-4574-8D2A-C7B46A86E3E8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54163960-175C75B0-90C1-4574-8D2A-C7B46A86E3E8
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type
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Statement
wasDerivedFrom
d3f6d3e1d8baac7970da4adf85b437fb01937a67
P2860
A recurrent 1.71 Mb genomic imbalance at 2q13 increases the risk of developmental delay and dysmorphism.