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Q50313091-2DFA4BB9-E691-4FC2-9CA7-881703A45487
Q50313091-2DFA4BB9-E691-4FC2-9CA7-881703A45487
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50313091-2DFA4BB9-E691-4FC2-9CA7-881703A45487
Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype.
P2860
Q50313091-2DFA4BB9-E691-4FC2-9CA7-881703A45487
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50313091-2DFA4BB9-E691-4FC2-9CA7-881703A45487
rank
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type
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Statement
wasDerivedFrom
bace0fbf2eddf26114f2613d656c96fe1a99b24b
P2860
A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome