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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Detalles Bibliográficos
Autor principal: Skomorowsky, Anne (-)
Otros Autores: Hagerman, Randi Jenssen, 1949-
Formato: Libro electrónico
Idioma:Inglés
Publicado: New York : Columbia University Press [2022]
Colección:EBSCO Academic eBook Collection Complete.
Acceso en línea:Conectar con la versión electrónica
Ver en Universidad de Navarra:https://innopac.unav.es/record=b4744180x*spi

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