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HMGA2

MIM.600698 12q14-q15

 

Pathology

-  truncated HMGA2 isoforms

-  chromosomal translocations

-  myelodyplasia

-  HMGA2 fusion genes

-  constitutional rearrangement of HMGA2 in a phenotype including extreme somatic overgrowth, advanced endochondral bone and dental ages, a cerebellar tumor, and multiple lipomas (#15593017#)


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