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Q38315593-A73DBBFA-0298-4F6C-9003-C22FCB83875C
Q38315593-A73DBBFA-0298-4F6C-9003-C22FCB83875C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38315593-A73DBBFA-0298-4F6C-9003-C22FCB83875C
Multilocus methylation defects in imprinting disorders.
P2860
Q38315593-A73DBBFA-0298-4F6C-9003-C22FCB83875C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38315593-A73DBBFA-0298-4F6C-9003-C22FCB83875C
rank
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wasDerivedFrom
825938fc697691ea382315c60e3f6fc7a2ca22de
P2860
A new deletion ablating NESP55 causes loss of maternal imprint of A/B GNAS and autosomal dominant pseudohypoparathyroidism type Ib