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Q38308028-07B3A8E8-EE52-476F-8A92-D11830A0FE13
Q38308028-07B3A8E8-EE52-476F-8A92-D11830A0FE13
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-07B3A8E8-EE52-476F-8A92-D11830A0FE13
Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.
P356
Q38308028-07B3A8E8-EE52-476F-8A92-D11830A0FE13
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-07B3A8E8-EE52-476F-8A92-D11830A0FE13
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
324cc81a4b35eb42a2b209557be285df17a36099
P356
10.1093/HMG/DDU144
http://www.w3.org/2001/XMLSchema#string
P356
DDU144