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Q38308028-EEDBAD1A-5E7A-435B-9B74-0EE2610F0D71
Q38308028-EEDBAD1A-5E7A-435B-9B74-0EE2610F0D71
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-EEDBAD1A-5E7A-435B-9B74-0EE2610F0D71
Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.
P921
Q38308028-EEDBAD1A-5E7A-435B-9B74-0EE2610F0D71
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-EEDBAD1A-5E7A-435B-9B74-0EE2610F0D71
rank
NormalRank
type
BestRank
Statement
P921
birth defect