What Does We Know of Chromosome X Fragile

Dra Mirta D'Ambra
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Dra Mirta D'Ambra: Buenos Aires University, Argentina

Biomedical Journal of Scientific & Technical Research, 2017, vol. 1, issue 3, 703-704

Abstract: Chromosome X Fragile is the prevalent hereditary cause of intellectual disability. It is an inherited disease linked to the X chromosome, Fragile X syndrome (S X F). Its main clinical manifestation is intellectual disability and affects mainly males, with a prevalence of 1/4000 and females 1/6000...

Keywords: Biomedical Sciences; Biomedical Research; Technical Research (search for similar items in EconPapers)
Date: 2017
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Persistent link: https://EconPapers.repec.org/RePEc:abf:journl:v:1:y:2017:i:3:p:703-704

DOI: 10.26717/BJSTR.2017.01.000280

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