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Q37693348-8806629C-EADC-4BB6-89F6-EB7B4EA4F1AE
Q37693348-8806629C-EADC-4BB6-89F6-EB7B4EA4F1AE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37693348-8806629C-EADC-4BB6-89F6-EB7B4EA4F1AE
Rare variants in NR2F2 cause congenital heart defects in humans.
P2860
Q37693348-8806629C-EADC-4BB6-89F6-EB7B4EA4F1AE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37693348-8806629C-EADC-4BB6-89F6-EB7B4EA4F1AE
rank
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wasDerivedFrom
06121e0f54576ad0eeddc9feed8778eadcf90917
P2860
Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization