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Q41691206-A90166E7-1F53-41FC-A4A9-30F8036253A6
Q41691206-A90166E7-1F53-41FC-A4A9-30F8036253A6
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Statement
http://www.wikidata.org/entity/statement/Q41691206-A90166E7-1F53-41FC-A4A9-30F8036253A6
A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndrome.
P1433
Q41691206-A90166E7-1F53-41FC-A4A9-30F8036253A6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41691206-A90166E7-1F53-41FC-A4A9-30F8036253A6
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wasDerivedFrom
5e26e625ada3c9c63006a1eb92ae29ea6c7d1bb9
P1433
European Journal of Human Genetics