OMIM - Anemia

Homo sapiens |   Mutations/Phenotypic

This study contains curated human phenotype data extracted from OMIM. Additional computational processing and curation of the phenotype data was performed to further organize and group data from related phenotypes into unifying disease categories.

Source: NextBio Library/Mutation and Phenotypic data

Kidney from patients with normal and dysfunctional renal allografts

Homo sapiens |   RNA Expression

We used DNA microarrays in a systematic study of gene-expression patterns in biopsy samples from normal and dysfunctional renal allografts.

Authors: Sarwal Minnie

Organization: Stanford University Biochemistry Brown S…