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Q34190554-AD4EFD48-F68F-4DFA-83F8-99FE0A20B2D3
Q34190554-AD4EFD48-F68F-4DFA-83F8-99FE0A20B2D3
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http://www.wikidata.org/entity/statement/Q34190554-AD4EFD48-F68F-4DFA-83F8-99FE0A20B2D3
The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome.
P2860
Q34190554-AD4EFD48-F68F-4DFA-83F8-99FE0A20B2D3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34190554-AD4EFD48-F68F-4DFA-83F8-99FE0A20B2D3
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wasDerivedFrom
ad7185173e4fa0f5c3f1b7ffd895423b51247de8
P2860
Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype.