GENETIC CHARACTERISTICS AND CLINICAL SIGNIFICANCE OF X CHROMOSOME-LINKED DISORDERS
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Abstract
This article discusses the genetic basis of X-linked hereditary diseases, their mechanisms of inheritance, clinical manifestations and relevance. The study analyzes the structure of the X chromosome, the genes located on it and their functional significance in the human body. Also, the genetic mechanisms of X-linked diseases such as hemophilia, Daltonism, Duchenne muscular dystrophy are explained through clinical examples. The article covers modern trends in early detection, genetic counseling and diagnostic methods for X-linked hereditary diseases.
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References
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