Fragile X Mental Retardation
- Author(s)
- Dr. Hossein Najmabadi, Dr. Mohammad Khalil Javan, Farbod Behboozadeh, Ramin Radpour, Mandana Hassanzad
- Year
- 2003
- Language
- Persian
- BISAC Code
- MED056000 — Medical / Genetics MED105000 — Medical / Neurology
- Scopus Subject Area
- Genetics, Molecular Biology, Neurology, Clinical Medicine, Developmental Disorders
- Target Audience
- Geneticists, neurologists, molecular biology researchers, clinicians, medical students, rehabilitation specialists
- Citation Info
- summary
- This book provides a molecular and genetic overview of Fragile X Syndrome, one of the most common hereditary causes of intellectual disability. It explains how scientific advances, from early cytogenetic observations to modern molecular diagnostics, have transformed understanding of this disorder. The introduction highlights the historical progression from early beliefs about disease to contemporary genetic research, emphasizing the role of dynamic mutations, trinucleotide repeat expansion, and the FMR1 gene. The book is part of a series produced by the university’s Genetics Research Center, aiming to present clear, accessible analyses of hereditary disorders for students and researchers in human molecular genetics.
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