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Q34297140-3A3588BA-1737-4F17-8CF4-DE71DCE5B690
Q34297140-3A3588BA-1737-4F17-8CF4-DE71DCE5B690
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http://www.wikidata.org/entity/statement/Q34297140-3A3588BA-1737-4F17-8CF4-DE71DCE5B690
Methylation defect in imprinted genes detected in patients with an Albright's hereditary osteodystrophy like phenotype and platelet Gs hypofunction
P2860
Q34297140-3A3588BA-1737-4F17-8CF4-DE71DCE5B690
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34297140-3A3588BA-1737-4F17-8CF4-DE71DCE5B690
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wasDerivedFrom
d7fe8605c45cd28a006cf72549ee8587c5ffd643
P2860
A new deletion ablating NESP55 causes loss of maternal imprint of A/B GNAS and autosomal dominant pseudohypoparathyroidism type Ib