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Q58869324-AF71CEE4-17BD-48D9-9516-320921B9D2AF
Q58869324-AF71CEE4-17BD-48D9-9516-320921B9D2AF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58869324-AF71CEE4-17BD-48D9-9516-320921B9D2AF
A de novo interstitial deletion of 2p23.3-24.3 in a boy presenting with intellectual disability, overgrowth, dysmorphic features, skeletal myopathy, dilated cardiomyopathy
P2860
Q58869324-AF71CEE4-17BD-48D9-9516-320921B9D2AF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58869324-AF71CEE4-17BD-48D9-9516-320921B9D2AF
rank
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type
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wasDerivedFrom
a868db053df89b093eb3f7d88bead1a0c09a5136
P2860
Deletion 2p25.2: a cryptic chromosome abnormality in a patient with autism and mental retardation detected using aCGH.