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1
Q38308028-722ADB68-A2A4-4006-B295-D5CE9652D780
Q38308028-722ADB68-A2A4-4006-B295-D5CE9652D780
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-722ADB68-A2A4-4006-B295-D5CE9652D780
Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.
P698
Q38308028-722ADB68-A2A4-4006-B295-D5CE9652D780
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-722ADB68-A2A4-4006-B295-D5CE9652D780
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
324cc81a4b35eb42a2b209557be285df17a36099
P698
24694933
http://www.w3.org/2001/XMLSchema#string