OMIM - Congenital disorder

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

Total # Biosets: 614

Gene expression in neuroblastomas with recurrent genomic alterations

Gene expression analysis was performed on 30 Neuroblastomas to identify genes whose transcription is significantly altered by recurrent chromosomal alterations.

Authors: Jackson S Michael, Lastowska Maria

Organization: Newcastle University Institute of Human …

Total # Biosets: 9