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The Genetic Basis of Common Diseases No. 20 (1992, Hardcover)

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eBay item number:392273191072
Last updated on Jul 07, 2021 08:35:36 PDTView all revisionsView all revisions

Item specifics

Condition
Very Good: A book that does not look new and has been read but is in excellent condition. No obvious ...
Modified Item
No
Bundle
No
Year
1992
Non-Domestic Product
No
ISBN
9780195054828
EAN
9780195054828
Publication Name
Genetic Basis of Common Diseases
Item Length
11.2in
Publisher
Oxford University Press, Incorporated
Publication Year
1992
Series
Oxford Monographs on Medical Genetics Ser.
Type
Textbook
Format
Hardcover
Language
English
Item Height
1.9in
Author
Jerome I. Rotter
Item Width
8.7in
Item Weight
87.5 Oz
Number of Pages
992 Pages

About this product

Product Information

Here is a unique and comprehensive resource for human geneticists and physicians concerned with the genetic causes of diseases routinely seen in research, clinical practice, and genetic counseling. Each of the chapters covers a particular disease, describes the genetic factors involved, and define the relevant biochemical, immunological, and physiological markers. The expert, widely known contributors also detail clinical applications, with advice on how the genetic data can be used to evaluate individuals and families, interpret diagnostic texts, and manage the disease.

Product Identifiers

Publisher
Oxford University Press, Incorporated
ISBN-10
0195054822
ISBN-13
9780195054828
eBay Product ID (ePID)
50209

Product Key Features

Author
Jerome I. Rotter
Publication Name
Genetic Basis of Common Diseases
Format
Hardcover
Language
English
Publication Year
1992
Series
Oxford Monographs on Medical Genetics Ser.
Type
Textbook
Number of Pages
992 Pages

Dimensions

Item Length
11.2in
Item Height
1.9in
Item Width
8.7in
Item Weight
87.5 Oz

Additional Product Features

Series Volume Number
No. 20
Lc Classification Number
Rb155.G3593 1992
Reviews
"This useful reference text is not only relevant to the student seeking abasic understanding of a particular disease, it is relevant to the physicianthrough its discussion of treatments and to the genetic counselor through itspresentation of genetic risk information for families. It can also serve as asummary of research findings for investigators not working directly with aparticular disease....Covers such a broad array of human diseases that it couldserve as a supplement to courses in medical genetics or human genetics....A verysolid reference text..." --Richard H. Myers, PhD (Boston University School ofMedicine), Amyloid: International Journal of Experimental and ClinicalInvestigation, "An up-to-date discussion of the issues. For any epidemiologist working ina field where an autoimmune mechanism has been suggested, reading these chaptersis an obligation. . . . this book has an important place as a reference book inlibraries of public health." --Roberto Rona, American Journal ofEpidemiology, "Follows the tradition of excellence of the Oxford Monographs on MedicalGenetics series. . . . this text is welcome as it provides a comprehensivereview of the current state of understanding of the genetic basis of many of thecommon diseases. . . . an essential reference to have in a departmentallibrary." --R.F. Mueller (St. James's University Hospital, UK), NeuromuscularDisorders, "Comprehensive....Future generations of physicians may look back at thefirst edition of this book much the way we now perceive Osler's Priciples andPractice of Medicine, ...- as the first in a long line of episodic revisionsthat acquired many competitors along the way....The chapter on genetics andinfectious diseases...is a real gem." Reed E. Pyeritz, MD, PhD, Allegheny-SingerResearch Institute, --Annals of Internal Medicine, "The first few chapters comprise a primer in contemporary human geneticmethods. All are well referenced. This is a timely and lucid summary of currentunderstanding of remaining challenges in human genetics." --Donald L. Rucknagel(University of Cincinnati College of Medicine), American Journal of HumanGenetics, "An excellent compilation of current knowledge....The chapters are well organized and referenced....Provides an extremely useful assessment of genetic aspects of many common disorders....Should interest all geneticists, internists, and specialists in the disorders considered. The binding andlayout, including photographs, are exceptionally good, typical of the best from Oxford and reflected in the price. I use this fine book daily and look forward to subsequent editions." --Stephen Kahler, MD, JAMA, "Follows the tradition of excellence of the Oxford Monographs on Medical Genetics series. . . . this text is welcome as it provides a comprehensive review of the current state of understanding of the genetic basis of many of the common diseases. . . . an essential reference to have in adepartmental library." --R.F. Mueller (St. James's University Hospital, UK), Neuromuscular Disorders, "The first few chapters comprise a primer in contemporary human genetic methods. All are well referenced. This is a timely and lucid summary of current understanding of remaining challenges in human genetics." --Donald L. Rucknagel (University of Cincinnati College of Medicine), AmericanJournal of Human Genetics, "An up-to-date discussion of the issues. For any epidemiologist working in a field where an autoimmune mechanism has been suggested, reading these chapters is an obligation. . . . this book has an important place as a reference book in libraries of public health." --Roberto Rona, AmericanJournal of Epidemiology, "Comprehensive....Future generations of physicians may look back at the first edition of this book much the way we now perceive Osler's Priciples and Practice of Medicine, ...- as the first in a long line of episodic revisions that acquired many competitors along the way....The chapter ongenetics and infectious diseases...is a real gem." Reed E. Pyeritz, MD, PhD, Allegheny-Singer Research Institute, --Annals of Internal Medicine, "Comprehensive....Future generations of physicians may look back at thefirst edition fo this book much the way we now perceive Osler's Priciples andPractice of Medicine, ...- as the first in a long line of episodic revisionsthat acquired many competitors along the way....The chapter on genetics andinfectious diseases...is a real gem." Reed E. Pyeritz, MD, PhD, Allegheny-SingerResearch Institute, --Annals of Internal Medicine, "This useful reference text is not only relevant to the student seeking a basic understanding of a particular disease, it is relevant to the physician through its discussion of treatments and to the genetic counselor through its presentation of genetic risk information for families. It canalso serve as a summary of research findings for investigators not working directly with a particular disease....Covers such a broad array of human diseases that it could serve as a supplement to courses in medical genetics or human genetics....A very solid reference text..." --Richard H. Myers, PhD(Boston University School of Medicine), Amyloid: International Journal of Experimental and Clinical Investigation, "A timely resource. The authors extensively review available knowledge and the chapters are extremely well referenced. . . . a highly recommended reference source that should be acquired by medical libraries as well as genetic units. It contains a wealth of information that is difficult toreadily access elsewhere." --Genetic Services of Western Australia
Table of Content
PART I: Introduction: The Study of Common Disease1. The Approach to Genetic Bases of Common Diseases2. Molecular Genetics3. Human Gene Mapping, Linkage, and Association4. Analysis of Genetic Data: Methods and Interpretation5. Genetics and Infectious Diseases*n 67. Biologic Basis of Autoimmune Disease8. Allergy and Asthma9. The Genetics of Coronary Atherosclerosis10. Hypertension11. Structural Heart Disease12. Chronic Obstructive Pulmonary Disease13. Peptic Ulcer Disease14. Gluten-Sensitive Enteropathy15. Lactase Deficiency: Biologic and Medical Aspects of the Adult Human Lactase Polymorphism16. Inflammatory Bowel Disease17. Genetic Basis of Chronic Liver Diseases18. Common Hyperbilirubinemias19. Thyroid Disease20. Parathyroid Disease21. Diabetes Mellitus22. Hyperuricemia and Gout23. Obesity24. Disorders of Adrenal Steriodogenesis25. Renal Tract Malformations26. Gynecologic Disorders27. Infertility and Pregnancy Loss28. Rheumatoid Arthritis29. Connective Tissue Biology and Common Skeletal Disorders30. Cancer in Families31. Gastrointestinal Cancer32. Breast Cancer33. Lung Cancer34. Reproductive Organ Cancer35. Hematolgic Malignancies36. Epilepsy37. Demyelinating Disease38. Parkinson's Disease39. Alzheimer's Disease40. The Major Affective Disorders: Bipolar, Unipolar, and Schizoaffective41. Schizophrenia42. Alcoholism43. Panic Disorder44. Klinefelter's Syndrome45. Turner Syndrome46. Longevity and Aging
Copyright Date
1992
Topic
Genetics, General
Lccn
90-007643
Dewey Decimal
616.042
Intended Audience
Scholarly & Professional
Dewey Edition
21
Illustrated
Yes
Genre
Medical

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