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Q53204200-E7519BF7-D3DC-4201-B229-0F757781B505
Q53204200-E7519BF7-D3DC-4201-B229-0F757781B505
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53204200-E7519BF7-D3DC-4201-B229-0F757781B505
Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes.
P2860
Q53204200-E7519BF7-D3DC-4201-B229-0F757781B505
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53204200-E7519BF7-D3DC-4201-B229-0F757781B505
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wasDerivedFrom
11a0bf76638e68850f51c2bfba9804cdb50d6987
P2860
Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.