The carriers what the fragile X gene reveals about family, heredity, and scientific discovery
"Fragile X syndrome is a genetic condition that causes a range of neurodevelopmental problems including learning disabilities and cognitive impairment. Boys with the condition are more likely to be born fully affected by it, while women who are seemingly unaffected carriers have an increased ri...
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| Formato: | Libro electrónico |
| Idioma: | Inglés |
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New York :
Columbia University Press
[2022]
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| Colección: | EBSCO Academic eBook Collection Complete.
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| Acceso en línea: | Conectar con la versión electrónica |
| Ver en Universidad de Navarra: | https://innopac.unav.es/record=b4744180x*spi |
Tabla de Contenidos:
- One damn thing after another
- Fragile X mutations : an overview
- Village of fools : how carriers brought fragile X to the new world, and what happened next
- A classic zebra : fragile X-associated primary ovarian insufficiency (FXPOI)
- The movement disorder that started a movement : fragile X-associated tremor/ataxia syndrome (FXTAS)
- Once more, with feelings : fragile X-associated neuropsychiatric disorders (FXAND)
- What are fragile eggs? : to test or not to test
- Borderlands of the premutation : gray zones, low-normals, and endophenotypes
- Outcomes.
