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Q24676539-20E3262A-4256-4EEB-B7AB-4B102424FEAF
Q24676539-20E3262A-4256-4EEB-B7AB-4B102424FEAF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24676539-20E3262A-4256-4EEB-B7AB-4B102424FEAF
Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms
P2860
Q24676539-20E3262A-4256-4EEB-B7AB-4B102424FEAF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24676539-20E3262A-4256-4EEB-B7AB-4B102424FEAF
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wasDerivedFrom
551cb201ba0717380ee4f42a7bcc92f24e70969e
P2860
Two 22q telomere deletions serendipitously detected by FISH