Analysis of Triplet Repeat Disorders, (Human Molecular Genetics) - Hardcover

9780122204319: Analysis of Triplet Repeat Disorders, (Human Molecular Genetics)
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The clinical picture of diseases, caused by trinucleotide repeats, such as fragile X syndrome, myotonic dystrophy, Huntington's disease and forms of spinocerebella ataxia, provide the starting point for this authoritative review volume.
The book proceeds to integrate the current understanding of the molecular pathologies of these diseases, their genotype-phenotype relationships, the mutational processes involved and the laboratory and clinical issues relating to genetic testing for these disorders.
Clinicians and researchers in genetics, neuroscience, pediatrics and psychiatry will all benefit from the comprehensive overviews contributed by recognized world experts.

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  • PublisherAcademic Press
  • Publication date2007
  • ISBN 10 012220431X
  • ISBN 13 9780122204319
  • BindingHardcover
  • Number of pages250

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9781859962664: Analysis of Triplet Repeat Disorders (Human Molecular Genetics)

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ISBN 10:  1859962661 ISBN 13:  9781859962664
Publisher: Garland Science, 1998
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