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Q47103314-01F0BAD2-BAB6-465A-A4EA-4506DC5B2287
Q47103314-01F0BAD2-BAB6-465A-A4EA-4506DC5B2287
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http://www.wikidata.org/entity/statement/Q47103314-01F0BAD2-BAB6-465A-A4EA-4506DC5B2287
De novo paternal origin duplication of chromosome 11p15.5: report of two Chinese cases with Beckwith-Wiedemann syndrome.
P2860
Q47103314-01F0BAD2-BAB6-465A-A4EA-4506DC5B2287
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47103314-01F0BAD2-BAB6-465A-A4EA-4506DC5B2287
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wasDerivedFrom
369d919335b439d193cbd530b997c9e59b069694
P2860
NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits.