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Q47562035-B1A40C47-D7F4-4CDB-89A9-E2A4ABC1DAA0
Q47562035-B1A40C47-D7F4-4CDB-89A9-E2A4ABC1DAA0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47562035-B1A40C47-D7F4-4CDB-89A9-E2A4ABC1DAA0
Framework for assessing individuals with rare genetic disorders associated with profound intellectual and multiple disabilities (PIMD): the example of Phelan McDermid Syndrome.
P2860
Q47562035-B1A40C47-D7F4-4CDB-89A9-E2A4ABC1DAA0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47562035-B1A40C47-D7F4-4CDB-89A9-E2A4ABC1DAA0
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wasDerivedFrom
f0eb39e0d60d334222488d732f115c82f359e692
P2860
Developmental phenotype in Phelan-McDermid (22q13.3 deletion) syndrome: a systematic and prospective study in 34 children.