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cgg
- 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- ...
- 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 ...
- ... 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 ...
- ... 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 ...
- ... 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 ...
- ... 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 ...
- Learning about Fragile X Syndrome (National Human Genome Research Institute)Fragile X Syndrome/Start Here ... Fragile X Syndrome ... Fragile X syndrome is an inherited intellectual disability caused by a mutation in the FMR1 gene. ... National ...
- Fragile X-Associated Disorders (FXD): A Handbook for Families, Health Care Providers, Counselors, and Educators (National Fragile X Foundation) - PDFFragile X Syndrome/Start Here ... Fragile X Syndrome ... National Fragile X Foundation ... PDF ... fragile x, handbook, 3rd edition, NFXF
- Fragile X Syndrome: Other FAQs (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 ...
- ... dystrophy type 1: role of CCG, CTC and CGG interruptions within DMPK alleles in the pathogenesis and ...