Results 1 -
10
of
29
for
Segment
- Learning about Fragile X Syndrome (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 ...
- Talking Glossary of Genetic Terms (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 ...
- GeneReviews Glossary (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 ...
- Annual Report to the Nation on the Status of Cancer, 1975-2014, Featuring Survival (National Cancer Institute)Cancer/Statistics and Research ... Cancer ... National Cancer Institute ... From the National Institutes of Health ... AbstractBackground. The American Cancer Society (ACS), ...
- Chromosome Abnormalities (National Human Genome Research Institute)Genetic Disorders/Reference Desk ... Genetic Disorders ... National Human Genome Research Institute ... From the National Institutes of Health ... Chromosome abnormalities ...
- Brief Guide to Genomics: DNA, Genes and Genomes (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 ...
- Deep Brain Stimulation (DBS) for the Treatment of Parkinson's Disease and other Movement Disorders (National Institute of Neurological Disorders and Stroke)Movement Disorders/Statistics and Research ... Movement Disorders ... Parkinson's Disease/Statistics and Research ... Parkinson's Disease ... National Institute of Neurological ...
- About Myotonic Dystrophy (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
- About Antiphospholipid Syndrome (APS) (National Human Genome Research Institute)Autoimmune Diseases/Specifics ... Autoimmune Diseases ... National Human Genome Research Institute ... From the National Institutes of Health ... Antiphospholipid Syndrome ...
- Genes and Disease: Prader-Willi Syndrome (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 ( ...