Details

Subject(s)

• Human molecular genetics [Browse]
• Genetic disorders [Browse]
• Human genome [Browse]

Summary note

"The Second Edition of this internationally acclaimed text expands its coverage of the molecular genetics of inherited human diseases with the latest research findings and discoveries. Using a unique, systems-based approach, the text offers readers a thorough explanation of the gene discovery process and how defective genes are linked to inherited disease states in major organ and tissue systems. All the latest developments in functional genomics, proteomics, and microarray technology have been thoroughly incorporated into the text." "This text is targeted at upper-level undergraduate students, graduate students, and medical students. It is also an excellent reference for researchers and physicians who need a clinically relevant reference for the molecular genetics of inherited human diseases."--Jacket.

Bibliographic references

Includes bibliographical references and index.

Contents

• Understanding human disease
• The genetic system: chromosomes
• The genetic system: Mendel's law of inheritance and genetic linkage
• The molecular biology of the gene
• Recombinant DNA technology
• Genetic and physical mapping of the human genome
• Discovering human disease genes
• Bioinformatics: genomics, functional genomics, and proteomics
• Human population genetics
• Molecular genetics of complex disorders
• Genomic imprinting: an epigenetic modification
• Molecular genetics of mitochondrial disorders
• Molecular genetics of muscle disorders
• Molecular genetics of neurological disorders
• Molecular genetics of the eye
• Molecular genetics of cancer syndromes
• Counseling, diagnostic testing, and management of genetic disorders.

Show 14 more Contents items

ISBN

• 0471474266
• 9780471474265

LCCN

2005278472

OCLC

58830127

Doi

• 10.1002/0471719188

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