Molecular Genetic Medicine: v. 2

Molecular Genetic Medicine: v. 2

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This serial presents critical reviews that inform basic scientists and medical researchers of progress in genetic medicine and its applications. It includes technical and historical overviews of molecular biology applied to disease detection, diagnosis, and treatment, and chronicles the continuing explosion of knowledge in molecular genetic medicine, giving current approaches to understanding human illness.
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Product details

  • Hardback | 233 pages
  • 165.1 x 230 x 19.05mm | 590g
  • Academic Press Inc
  • San Diego, United States
  • English
  • references, index
  • 0124620027
  • 9780124620025

Table of contents

The impact of molecular biology in the diagnosis and treatment of hemoglobin disorders, P.E. Berg and A.N. Schechter; the fragile X syndrome, W.T. Brown and E.C. Jenkins; hepatitis B virus biology and pathogenesis, F. Chisari; the molecular genetics of down syndrome, D.M. Holtzman and C.J. Epstein; mammalian X chromosome inactivation, S.M. Gartler, et al; molecular analysis of mutation in the human gene for hypoxanthine phosphoribosyltransferase, B. Lambert, et al; regulatory genes of human immunodeficiency viruses, F. Wong-Staal and W.A. Haseltine.
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