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Results 1 - 10 of 33 for Codon
  1. Talking Glossary of Genetic Terms From the National Institutes of Health (National Human Genome Research Institute)  
    Birth Defects/Reference Desk ... Birth Defects ... Genes and Gene Therapy/Reference Desk ... Genes and Gene Therapy ... Genetic Disorders/Reference Desk ... Genetic Disorders ... Genetic ...
  2. ... nucleotides. Each sequence of three nucleotides, called a codon, usually codes for one particular amino acid. (Amino ... assembly continues until the ribosome encounters a “stop” codon (a sequence of three nucleotides that does not ...
  3. ... O, Hefter H, Korth C. Prion protein gene codon 129 modulates clinical course of neurological Wilson disease. ... Gessner R. Influence of homozygosity for methionine at codon 129 of the human prion gene on the ...
  4. Risk Factors for Eye Cancer (American Cancer Society)  
    Eye Cancer/Prevention and Risk Factors ... Eye Cancer ... American Cancer Society ... Certain risk factors may increase your chance of developing eye cancer. This guide ...
  5. GeneReviews Glossary From the National Institutes of Health (National Center for Biotechnology Information)  
    Genetic Testing/Reference Desk ... Genetic Testing ... Newborn Screening/Reference Desk ... Newborn Screening ... National Center for Biotechnology Information ... From the National ...
  6. Eye Cancer/Statistics and Research ... Eye Cancer ... American Cancer Society ... Research into causes, prevention and treatment of eye cancer is ongoing in many medical ...
  7. Creutzfeldt-Jakob Disease (Alzheimer's Association)  
    Creutzfeldt-Jakob Disease/Start Here ... Creutzfeldt-Jakob Disease ... Alzheimer's Association ... Creutzfeldt-Jakob disease – learn about CJD symptoms, diagnosis, causes ...
  8. ... A, Cormier-Daire V. Mutations at a single codon in Mad homology 2 domain of SMAD4 cause ...
  9. ... HR. A mutation creating an upstream translation initiation codon in SLC22A5 5'UTR is a frequent cause ...
  10. ... cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 ...
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