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Q38308028-DE13AECD-7C5E-4337-B98D-D041ACAD33A7
Q38308028-DE13AECD-7C5E-4337-B98D-D041ACAD33A7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-DE13AECD-7C5E-4337-B98D-D041ACAD33A7
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-DE13AECD-7C5E-4337-B98D-D041ACAD33A7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-DE13AECD-7C5E-4337-B98D-D041ACAD33A7
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
324cc81a4b35eb42a2b209557be285df17a36099
P1545
7
http://www.w3.org/2001/XMLSchema#string
P2093
Thor Thorsson
http://www.w3.org/2001/XMLSchema#string