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Q38308028-C7C9082E-2404-4FDA-912C-58B0C9BA507B
Q38308028-C7C9082E-2404-4FDA-912C-58B0C9BA507B
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Statement
http://www.wikidata.org/entity/statement/Q38308028-C7C9082E-2404-4FDA-912C-58B0C9BA507B
Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.
P2860
Q38308028-C7C9082E-2404-4FDA-912C-58B0C9BA507B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-C7C9082E-2404-4FDA-912C-58B0C9BA507B
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wasDerivedFrom
2fd4d693cd71e5da7aa3d5ff043f5adcf713aecc
P2860
A recurrent 1.71 Mb genomic imbalance at 2q13 increases the risk of developmental delay and dysmorphism.