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Q48173896-F238A2CB-1A3E-4019-A14D-631316E43729
Q48173896-F238A2CB-1A3E-4019-A14D-631316E43729
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http://www.wikidata.org/entity/statement/Q48173896-F238A2CB-1A3E-4019-A14D-631316E43729
Prenatal diagnosis of susceptibility loci for neurodevelopmental disorders - genetic counseling and pregnancy outcome in 57 cases.
P2860
Q48173896-F238A2CB-1A3E-4019-A14D-631316E43729
BestRank
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http://www.wikidata.org/entity/statement/Q48173896-F238A2CB-1A3E-4019-A14D-631316E43729
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2029b58995ff058a27bb08c869d5530449979d86
P2860
Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.