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Q34386278-7A8F7FA5-ED1B-46E1-ADAE-7DF92AF080B7
Q34386278-7A8F7FA5-ED1B-46E1-ADAE-7DF92AF080B7
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Statement
http://www.wikidata.org/entity/statement/Q34386278-7A8F7FA5-ED1B-46E1-ADAE-7DF92AF080B7
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis
P2860
Q34386278-7A8F7FA5-ED1B-46E1-ADAE-7DF92AF080B7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34386278-7A8F7FA5-ED1B-46E1-ADAE-7DF92AF080B7
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type
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wasDerivedFrom
ab12e6c1979482c02dd168e6d3061b717dcc8857
P2860
Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes