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Results 1 - 10 of 11 for cgg
  1. Features of Fragile X Syndrome (National Fragile X Foundation)  
    Fragile X Syndrome/Symptoms ... Fragile X Syndrome ... National Fragile X Foundation ... Fragile X Syndrome is caused by a full mutation of the FMR1 gene. Fragile X- ...
    https://fragilex.org/understanding-fragile-x/fragile-x-101 - External Health Links
  2. What It Means to be a Carrier (National Fragile X Foundation)  
    Fragile X Syndrome/Genetics ... Fragile X Syndrome ... National Fragile X Foundation ... Extensive information on Fragile X premutation carriers - what it means, what ...
    https://fragilex.org/.../fragile-x-101/premutation-carriers - External Health Links
  3. FMR1 gene 
    ... contains a particular DNA segment known as a CGG trinucleotide repeat, so called because this segment of ... the gene. In most people, the number of CGG repeats ranges from fewer than 10 to about ...
    https://medlineplus.gov/genetics/gene/fmr1 - Genetics
  4. Fragile X syndrome 
    ... in which a DNA segment, known as the CGG triplet repeat, is expanded within the FMR1 gene. ... In people with fragile X syndrome, however, the CGG segment is repeated more than 200 times. The ...
    https://medlineplus.gov/genetics/condition/fragile-x-syndrome - Genetics
  5. Fragile X-associated primary ovarian insufficiency 
    ... in which a DNA segment, known as a CGG triplet repeat, is expanded within the FMR1 gene. ... 40 times. In women with FXPOI, however, the CGG segment is repeated 55 to 200 times. This ...
    https://medlineplus.gov/...-associated-primary-ovarian-insufficiency - Genetics
  6. Fragile X-associated tremor/ataxia syndrome 
    ... in which a DNA segment, known as a CGG triplet repeat, is expanded within the FMR1 gene. ... 40 times. In people with FXTAS, however, the CGG segment is repeated 55 to 200 times. This ...
    https://medlineplus.gov/...agile-x-associated-tremor-ataxia-syndrome - Genetics
  7. 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 ...
    https://www.genome.gov/Genetic-Disorders/Fragile-X-Syndrome - External Health Links
  8. Fragile X-Associated Disorders (FXD): A Handbook for Families, Health Care Providers, Counselors, and Educators (National Fragile X Foundation) - PDF  
    Fragile X Syndrome/Start Here ... Fragile X Syndrome ... National Fragile X Foundation ... PDF ... fragile x, handbook, 3rd edition, NFXF
    https://fragilex.org/.../2012/01/Handbook-FXD_3rd_Edition.pdf - External Health Links
  9. Fragile X Syndrome: Other FAQs From the National Institutes of Health (Eunice Kennedy Shriver National Institute of Child Health and Human Development)  
    Fragile X Syndrome/Related Issues ... Fragile X Syndrome ... Eunice Kennedy Shriver National Institute of Child Health and Human Development ... From the National Institutes ...
    https://www.nichd.nih.gov/.../topics/fragilex/more_information/faqs - External Health Links
  10. DMPK gene 
    ... dystrophy type 1: role of CCG, CTC and CGG interruptions within DMPK alleles in the pathogenesis and ...
    https://medlineplus.gov/genetics/gene/dmpk - Genetics
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