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Q35230774-33B09A2C-8BD1-4476-8F4D-B926AA187559
Q35230774-33B09A2C-8BD1-4476-8F4D-B926AA187559
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Statement
http://www.wikidata.org/entity/statement/Q35230774-33B09A2C-8BD1-4476-8F4D-B926AA187559
Visual sensorial impairments in neurodevelopmental disorders: evidence for a retinal phenotype in Fragile X Syndrome
P2860
Q35230774-33B09A2C-8BD1-4476-8F4D-B926AA187559
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35230774-33B09A2C-8BD1-4476-8F4D-B926AA187559
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wasDerivedFrom
5b51cd571eec2cbd9b49d3d05fadd2c40052dbe4
P2860
Combined deletion of two Condensin II system genes (NCAPG2 and MCPH1) in a case of severe microcephaly and mental deficiency.