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Q38308028-C1D635E5-C672-4D86-9AED-B1AD7816FE11
Q38308028-C1D635E5-C672-4D86-9AED-B1AD7816FE11
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-C1D635E5-C672-4D86-9AED-B1AD7816FE11
Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.
P31
Q38308028-C1D635E5-C672-4D86-9AED-B1AD7816FE11
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-C1D635E5-C672-4D86-9AED-B1AD7816FE11
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type
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Statement
wasDerivedFrom
324cc81a4b35eb42a2b209557be285df17a36099
P31
scholarly article