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Q37716526-7E8C0B83-4D1E-4276-A970-FD1F40866CB2
Q37716526-7E8C0B83-4D1E-4276-A970-FD1F40866CB2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37716526-7E8C0B83-4D1E-4276-A970-FD1F40866CB2
Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes.
P2860
Q37716526-7E8C0B83-4D1E-4276-A970-FD1F40866CB2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37716526-7E8C0B83-4D1E-4276-A970-FD1F40866CB2
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type
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Statement
wasDerivedFrom
071cd119890ebc334ed6aa28d0887bbae80aeb14
P2860
Task-switching deficits and repetitive behaviour in genetic neurodevelopmental disorders: data from children with Prader-Willi syndrome chromosome 15 q11-q13 deletion and boys with Fragile X syndrome.