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Q41734111-9AC93C56-EE83-48D7-9CEE-1F78682433C3
Q41734111-9AC93C56-EE83-48D7-9CEE-1F78682433C3
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http://www.wikidata.org/entity/statement/Q41734111-9AC93C56-EE83-48D7-9CEE-1F78682433C3
Clinical utility gene card for: DiGeorge syndrome, velocardiofacial syndrome, Shprintzen syndrome, chromosome 22q11.2 deletion syndrome (22q11.2, TBX1).
P2860
Q41734111-9AC93C56-EE83-48D7-9CEE-1F78682433C3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41734111-9AC93C56-EE83-48D7-9CEE-1F78682433C3
rank
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wasDerivedFrom
9b2b0f81d586743b44b82e664c02c44a6f233aeb
P2860
Molecular mechanisms and diagnosis of chromosome 22q11.2 rearrangements