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Q34297140-F1753B44-0620-41CB-947E-8A9CC1B4F1FD
Q34297140-F1753B44-0620-41CB-947E-8A9CC1B4F1FD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34297140-F1753B44-0620-41CB-947E-8A9CC1B4F1FD
Methylation defect in imprinted genes detected in patients with an Albright's hereditary osteodystrophy like phenotype and platelet Gs hypofunction
P2860
Q34297140-F1753B44-0620-41CB-947E-8A9CC1B4F1FD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34297140-F1753B44-0620-41CB-947E-8A9CC1B4F1FD
rank
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type
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wasDerivedFrom
d7fe8605c45cd28a006cf72549ee8587c5ffd643
P2860
Prader-Willi syndrome and Angelman syndrome.