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Q33183177-B243084E-EB97-48C1-972C-DC1BFE671E25
Q33183177-B243084E-EB97-48C1-972C-DC1BFE671E25
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http://www.wikidata.org/entity/statement/Q33183177-B243084E-EB97-48C1-972C-DC1BFE671E25
Karyotype, phenotype and parental origin in 19 cases of triploidy.
P2860
Q33183177-B243084E-EB97-48C1-972C-DC1BFE671E25
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33183177-B243084E-EB97-48C1-972C-DC1BFE671E25
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wasDerivedFrom
d5920189c4c9e2d8059e550e57a823bc8d05a84d
P2860
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.