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Q36193242-70EE34EB-ACA6-431E-98DE-D610568D3388
Q36193242-70EE34EB-ACA6-431E-98DE-D610568D3388
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36193242-70EE34EB-ACA6-431E-98DE-D610568D3388
Clinical utility of array comparative genomic hybridisation in prenatal setting.
P2860
Q36193242-70EE34EB-ACA6-431E-98DE-D610568D3388
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36193242-70EE34EB-ACA6-431E-98DE-D610568D3388
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wasDerivedFrom
382985c93afe3ccf70449babe364d41d1002c347
P2860
Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.