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Q35533264-2FAA5219-D87C-4785-AF09-E72A15CC36D1
Q35533264-2FAA5219-D87C-4785-AF09-E72A15CC36D1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35533264-2FAA5219-D87C-4785-AF09-E72A15CC36D1
Contribution of copy-number variation to Down syndrome-associated atrioventricular septal defects.
P2860
Q35533264-2FAA5219-D87C-4785-AF09-E72A15CC36D1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35533264-2FAA5219-D87C-4785-AF09-E72A15CC36D1
rank
NormalRank
type
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Statement
wasDerivedFrom
4f65845e77da8a65755e733dd0e51b0056ab52e9
P2860
Rare variants in NR2F2 cause congenital heart defects in humans.