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Q36338177-114EC99D-E64B-43FE-8A90-37AF0C7A4F76
Q36338177-114EC99D-E64B-43FE-8A90-37AF0C7A4F76
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http://www.wikidata.org/entity/statement/Q36338177-114EC99D-E64B-43FE-8A90-37AF0C7A4F76
European guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS: an EQA study.
P2860
Q36338177-114EC99D-E64B-43FE-8A90-37AF0C7A4F76
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36338177-114EC99D-E64B-43FE-8A90-37AF0C7A4F76
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wasDerivedFrom
539477b91aa75d1cf46aa09675a6b5dfe9f21225
P2860
A new deletion ablating NESP55 causes loss of maternal imprint of A/B GNAS and autosomal dominant pseudohypoparathyroidism type Ib