Skip to Main Content

Paper Details

The unsolved rare genetic disease atlas? An analysis of the unexplained phenotypic descriptions in OMIM®.
Am J Med Genet C Semin Med Genet
21
2018
Author NameAffiliation
Taila HartleyChildren's Hospital of Eastern Ontario Research Institute, University of Ottawa
Kym M BoycottChildren's Hospital of Eastern Ontario Research Institute, University of Ottawa
Kym M BoycottChildren's Hospital of Eastern Ontario
  • 1 - 3

Datasets

Release 1.2