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Q54141361-1F00F2E1-E5AB-42EA-A05F-AC4C84D7F1E9
Q54141361-1F00F2E1-E5AB-42EA-A05F-AC4C84D7F1E9
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http://www.wikidata.org/entity/statement/Q54141361-1F00F2E1-E5AB-42EA-A05F-AC4C84D7F1E9
A novel Xp22.13 microdeletion in Nance-Horan syndrome.
P2860
Q54141361-1F00F2E1-E5AB-42EA-A05F-AC4C84D7F1E9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54141361-1F00F2E1-E5AB-42EA-A05F-AC4C84D7F1E9
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wasDerivedFrom
a45a945b6233c96e40e9f189e2073b904b661882
P2860
Encephalopathy and bilateral cataract in a boy with an interstitial deletion of Xp22 comprising the CDKL5 and NHS genes.