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Q34148921-42EE9647-2019-431E-A566-F5AB3625E5A2
Q34148921-42EE9647-2019-431E-A566-F5AB3625E5A2
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http://www.wikidata.org/entity/statement/Q34148921-42EE9647-2019-431E-A566-F5AB3625E5A2
An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome
P2860
Q34148921-42EE9647-2019-431E-A566-F5AB3625E5A2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34148921-42EE9647-2019-431E-A566-F5AB3625E5A2
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wasDerivedFrom
f74e79fa765ef8b9d448c50dbae0aabe86d81107
P2860
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11.