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Q35836803-8C28E6A0-529F-41DD-8C86-C0CF29247C2C
Q35836803-8C28E6A0-529F-41DD-8C86-C0CF29247C2C
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http://www.wikidata.org/entity/statement/Q35836803-8C28E6A0-529F-41DD-8C86-C0CF29247C2C
Methylation-specific multiplex ligation-dependent probe amplification and identification of deletion genetic subtypes in Prader-Willi syndrome.
P2860
Q35836803-8C28E6A0-529F-41DD-8C86-C0CF29247C2C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35836803-8C28E6A0-529F-41DD-8C86-C0CF29247C2C
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b009fb2801086fd3dfca83d2a2449665448eb1b7
P2860
Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.