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Q34957544-4549AFB9-0C0E-407C-9CA9-9443B7CFD690
Q34957544-4549AFB9-0C0E-407C-9CA9-9443B7CFD690
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Statement
http://www.wikidata.org/entity/statement/Q34957544-4549AFB9-0C0E-407C-9CA9-9443B7CFD690
Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype.
P1433
Q34957544-4549AFB9-0C0E-407C-9CA9-9443B7CFD690
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34957544-4549AFB9-0C0E-407C-9CA9-9443B7CFD690
rank
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type
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wasDerivedFrom
a80fdf3333c8485b15f780caa7569356dde8513e
P1433
Journal of Medical Genetics