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Q33409894-BAA23C8E-F177-41F0-A36F-26311BD77F95
Q33409894-BAA23C8E-F177-41F0-A36F-26311BD77F95
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33409894-BAA23C8E-F177-41F0-A36F-26311BD77F95
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.
P2860
Q33409894-BAA23C8E-F177-41F0-A36F-26311BD77F95
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33409894-BAA23C8E-F177-41F0-A36F-26311BD77F95
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
669ddefea0eabd75b598c78cc840df4128721829
P2860
Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy.