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Results 1 - 10 of 29 for Segment
  1. Learning about Fragile X Syndrome From the National Institutes of Health (National Human Genome Research Institute)  
    Fragile X syndrome is an inherited intellectual disability caused by a mutation in the FMR1 gene. ... Fragile X Syndrome/Start Here ... Fragile X Syndrome ... National ...
  2. 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 ...
  3. 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 ...
  4. Cancer/Statistics and Research ... Cancer ... National Cancer Institute ... From the National Institutes of Health ... AbstractBackground. The American Cancer Society (ACS), ...
  5. Chromosome Abnormalities From the National Institutes of Health (National Human Genome Research Institute)  
    Genetic Disorders/Reference Desk ... Genetic Disorders ... National Human Genome Research Institute ... From the National Institutes of Health ... Chromosome abnormalities ...
  6. Brief Guide to Genomics: DNA, Genes and Genomes From the National Institutes of Health (National Human Genome Research Institute)  
    Genes and Gene Therapy/Related Issues ... Genes and Gene Therapy ... National Human Genome Research Institute ... From the National Institutes of Health ... Genomics is the ...
  7. Movement Disorders/Statistics and Research ... Movement Disorders ... Parkinson's Disease/Statistics and Research ... Parkinson's Disease ... National Institute of Neurological ...
  8. About Myotonic Dystrophy From the National Institutes of Health (National Human Genome Research Institute)  
    Myotonic dystrophy is an inherited type of muscular dystrophy that affects the muscles and other body systems. ... Muscular Dystrophy/Genetics ... Muscular Dystrophy
  9. About Antiphospholipid Syndrome (APS) From the National Institutes of Health (National Human Genome Research Institute)  
    Autoimmune Diseases/Specifics ... Autoimmune Diseases ... National Human Genome Research Institute ... From the National Institutes of Health ... Antiphospholipid Syndrome ...
  10. Genes and Disease: Prader-Willi Syndrome From the National Institutes of Health (National Center for Biotechnology Information)  
    Prader-Willi Syndrome/Learn More ... Prader-Willi Syndrome ... National Center for Biotechnology Information ... From the National Institutes of Health ... Prader-Willi syndrome ( ...
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