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The Metabolic and Molecular Bases of Inherited Disease, 4 volume set
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The Metabolic and Molecular Bases of Inherited Disease, 4 volume set | Hardcover

by Barton Childs (Author), Arthur L. Beaudet (Author), David Valle (Author), Kenneth W. Kinzler (Author), Bert Vogelstein (Author), Charles R. Scriver (Editor), William S. Sly (Editor)

List Price: $709.00  
Price:  $567.20
You Save:  $141.80 (20%)
Available:  Usually ships in 11 to 14 days

Binding:  Hardcover
Publisher:  McGraw-Hill Professional
Edition:  8th Edition
Page Count:  6,338 Pages
Publication Date:  December 15, 2000
Sales Rank:  897,628th


EDITORIAL REVIEWS


Product Description
Authored by the most respected clinicians and researchers in the field, THE METABOLIC AND MOLECULAR BASES OF INHERITED DISEASE, 8th Edition, is the undisputed authority on genetic inheritance. In its pages, you can explore what is currently known about every inherited disease known to exist. Here you can review genetic perspectives, basic concepts, how inherited diseases occur, diagnostic approaches, and the effects of hormones. You can research specific syndromes, or read about specific body systems affected by disease. No other reference even comes close to its authority and comprehensive scope! * More than 50% totally new text and topics, with the remaining text totally written or updated to include the latest advances * Expanded coverage of cancer - from six chapters to more than three dozen - advances your knowledge of this explosive disease state and cancer genetics * New chapter on history of the inborn errors of metabolism * New chapter on the impact of inherited disease on health * New chapter on inherited diseases' response to treatment * New chapters relating to newly cloned genes * New insight on genetics' contribution to the understanding of complex traits and birth defects * Expanded coverage of neurogenetics * New information on comparative genomics and its relationship to the genome projects * New sections and chapters on disorders of human somatic development * Useful algorithms for diagnosing disorders of mitochondrial function and of mendelianclinical phenotypes


CUSTOMER REVIEWS (Average Customer Rating: 5.0 based on 1 review)

Comprehensive heavyweight 5 Stars
January 10, 2001
This is a suitably vast book for a vast subject. It covers every aspect of the application of human genetics to medicine, and the reviews are not only an ideal introduction to a genetic disease, but are heavily referenced as well. This makes it ideal as a guide to the most recent literature on the subject. The introductory chapters are essential reading as well.

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