OMIM diseases as a function of associated HPO phenotypes. Data include
Por um escritor misterioso
Descrição
The pace of disease gene discovery as cataloged by the OMIM Morbid
PhenPath: a tool for characterizing biological functions
Curation and expansion of Human Phenotype Ontology for defined
Solving patients with rare diseases through programmatic
GPCards: An integrated database of genotype–phenotype correlations
Comprehensive Analysis of Tissue-wide Gene Expression and
JPM, Free Full-Text
HPOSim: An R Package for Phenotypic Similarity Measure and
Integrative Data Mining Highlights Candidate Genes for Monogenic
Linking common human diseases to their phenotypes; development of
Genes, Free Full-Text
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