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Q36107483-349AA977-FEEC-4ED8-B7B2-8D4C86BCE93C
Q36107483-349AA977-FEEC-4ED8-B7B2-8D4C86BCE93C
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Statement
http://www.wikidata.org/entity/statement/Q36107483-349AA977-FEEC-4ED8-B7B2-8D4C86BCE93C
VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: the first description of a VAX1 phenotype in humans.
P2860
Q36107483-349AA977-FEEC-4ED8-B7B2-8D4C86BCE93C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36107483-349AA977-FEEC-4ED8-B7B2-8D4C86BCE93C
rank
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type
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wasDerivedFrom
63fb045f3840a8c08cdcf09010198305424c2614
P2860
Array comparative genomic hybridization in patients with congenital diaphragmatic hernia: mapping of four CDH-critical regions and sequencing of candidate genes at 15q26.1-15q26.2.