The study of human chromosomes, at both the microscopic and molecular level, has helped characterize many genetic diseases. As understanding of the etiology and mechanisms of cytogenetic disorders continues to increase, more families at risk for these diseases may be given help through genetic counselling, accurate risk estimation, and prenatal diagnosis. This new edition of Human Cytogenetics: A Practical Approach serves as a fully comprehensive manual of established cytogenetic protocols together with relevant background information. Volume I concentrates entirely on laboratory techniques used in the study and diagnosis of non-malignant chromosome abnormalities. It is an invaluable compendium of basic information and more advanced specialist techniques in cytogenetics.
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The study of human chromosomes has enabled us to characterize many genetic diseases and has provided the means to help many families at risk from these disorders. This volume is a manual of laboratory techniques used in the study and diagnosis of non-malignant chromosome abnormalities.
"About this title" may belong to another edition of this title.
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