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Results 1 - 10 of 1,066 for version cases
  1. ... settings will impede your use of the AWS version of MedlinePlus Connect after May 2023. In this case, please make the appropriate adjustments to your implementation ...
  2. ... This mutation results in an abnormally short, nonfunctional version of the enzyme. Another mutation causes most cases of the disorder in people of Finnish descent; ...
  3. ... of the gene, while others have the mutated version. This situation is called mosaicism. As in inherited cases, a second somatic mutation in the normal copy ...
  4. Skin Cancer Skin cancer cases Alternative accessible version (pdf) January 31, 2023 You May Also Like Dental Health Your smile (and mouth) can tell you more than you ...
  5. 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 Counseling/Reference Desk ... Genetic Counseling
  6. Sickle Cell Disease Association of America (Sickle Cell Disease Association of America)  
    ... Therapy & Bone Marrow Therapies Please note: A previous version of this advisory incorrectly stated that MARAC is aware of three cases of leukemia and other... Read more GBT and ...
  7. Rubella: Questions and Answers (Immunization Action Coalition) - PDF  
    Rubella/Start Here ... Rubella ... Immunization Action Coalition ... PDF ... rubella questions and answers information about the disease and vaccines, what you should know ...
  8. ... to the production of an abnormally small, nonfunctional version of the PAFAH1B1 protein. PAFAH1B1 gene mutations account for more than half of all ILS cases.PAFAH1B1 gene mutations cause PAF levels to be ...
  9. Cancer/Statistics and Research ... Cancer ... National Cancer Institute ... From the National Institutes of Health ... AbstractBackground. The American Cancer Society (ACS), ...
  10. ... protein. The mutations responsible for the milder, adult version of this disease usually change a single protein building block (amino acid) in the protein. In these cases, the altered protein may retain some function.People ...
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