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Q40352005-1A39787E-0144-4E37-BCDA-4960D7B50F69
Q40352005-1A39787E-0144-4E37-BCDA-4960D7B50F69
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http://www.wikidata.org/entity/statement/Q40352005-1A39787E-0144-4E37-BCDA-4960D7B50F69
The differentially methylated region of MEG8 is hypermethylated in patients with Temple syndrome.
P2860
Q40352005-1A39787E-0144-4E37-BCDA-4960D7B50F69
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40352005-1A39787E-0144-4E37-BCDA-4960D7B50F69
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69cfd5921faaa53c33d536d2234513d8a78878c1
P2860
Exclusion of maternal uniparental disomy of chromosome 14 in patients referred for Prader-Willi syndrome using a multiplex methylation polymerase chain reaction assay.