Molecular genetics of human inherited disease

著者

書誌事項

Molecular genetics of human inherited disease

edited by Duncan J. Shaw

（Molecular medical science series）

J. Wiley & Sons, c1995

大学図書館所蔵 件 / 全10件

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注記

Includes bibliographical references and index

内容説明・目次

内容説明

This is a summary of research advances which have implications for a number of diseases, including muscular dystrophy and cystic fibrosis. The text describes how these advances are leading to an understanding of the diseases' pathology, an essential first stage for devising treatment. The contributors also explain how knowledge gained through the discovery of various genes and associated mutations has enriched the wider field of genetics.

目次

  • Xp21 (Pseudohypertrophic) Muscular Dystrophy: Duchenne and Becker Muscular Dystrophy
  • The Cystic Fibrosis Gene: Cloning and Characterization
  • Huntington's Disease
  • The Fragile X Mental Retardation Syndrome
  • The Molecular Genetics of Myotonic Dystrophy
  • Genetic and Molecular Analysis of the Human Y Chromosome
  • Identification and Characterization of the Neurofibromatosis Type 1 Gene
  • The Genetics of Psychiatric Disorders.

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