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Q58700975-9C64BE4E-1454-44D8-A88D-2E0A7CA6A7BA
Q58700975-9C64BE4E-1454-44D8-A88D-2E0A7CA6A7BA
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http://www.wikidata.org/entity/statement/Q58700975-9C64BE4E-1454-44D8-A88D-2E0A7CA6A7BA
Importance and usage of chromosomal microarray analysis in diagnosing intellectual disability, global developmental delay, and autism; and discovering new loci for these disorders
P2860
Q58700975-9C64BE4E-1454-44D8-A88D-2E0A7CA6A7BA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58700975-9C64BE4E-1454-44D8-A88D-2E0A7CA6A7BA
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wasDerivedFrom
d999a16311c1012c598e8fe4534dca69ab0149e0
P2860
A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases.