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Q38308028-D76674C3-1A68-4A64-A757-47A01F127C01
Q38308028-D76674C3-1A68-4A64-A757-47A01F127C01
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-D76674C3-1A68-4A64-A757-47A01F127C01
Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.
P2093
Q38308028-D76674C3-1A68-4A64-A757-47A01F127C01
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-D76674C3-1A68-4A64-A757-47A01F127C01
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
324cc81a4b35eb42a2b209557be285df17a36099
P1545
1
http://www.w3.org/2001/XMLSchema#string
P2093
Mark W Russell
http://www.w3.org/2001/XMLSchema#string