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Q38308028-386F15B1-468C-4434-84E5-D2061A8C17E1
Q38308028-386F15B1-468C-4434-84E5-D2061A8C17E1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-386F15B1-468C-4434-84E5-D2061A8C17E1
Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.
P433
Q38308028-386F15B1-468C-4434-84E5-D2061A8C17E1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-386F15B1-468C-4434-84E5-D2061A8C17E1
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
324cc81a4b35eb42a2b209557be285df17a36099
P433
16
http://www.w3.org/2001/XMLSchema#string