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Q38308028-F3430AB7-9653-4F2B-B820-8FC0800C4295
Q38308028-F3430AB7-9653-4F2B-B820-8FC0800C4295
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-F3430AB7-9653-4F2B-B820-8FC0800C4295
Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.
P5875
Q38308028-F3430AB7-9653-4F2B-B820-8FC0800C4295
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-F3430AB7-9653-4F2B-B820-8FC0800C4295
rank
NormalRank
type
BestRank
Statement
P5875
261326345
http://www.w3.org/2001/XMLSchema#string