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Q37149716-11C19A6D-16B5-4583-9FCE-60166AB44031
Q37149716-11C19A6D-16B5-4583-9FCE-60166AB44031
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Statement
http://www.wikidata.org/entity/statement/Q37149716-11C19A6D-16B5-4583-9FCE-60166AB44031
A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus.
P2860
Q37149716-11C19A6D-16B5-4583-9FCE-60166AB44031
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37149716-11C19A6D-16B5-4583-9FCE-60166AB44031
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Statement
wasDerivedFrom
db93fab7c5ec580ac2f4d2a9ec3c00192c0982f5
P2860
A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10.