Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Fanconi anemia-like presentation in an infant with constitutional deletion of 21q including the RUNX1 gene.

Fanconi anemia-like presentation in an infant with constitutional deletion of 21q including the RUNX1 gene. . 2011 Jul; 155A(7):1673-9.

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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.