Mendelian Inheritance in Man: A Catalog of Human Genes and Genetic Disorders [3 volumes, complete] twelfth edition

McKusick MD, Victor A.; Antonarakis MD DSc, Stylianos E. [Assistant]; Francomano MD, Clair A. [Assistant]; Hurko MD, Orest [Assistant]; Scott PhD, Alan F. [Assistant]; Smith, Moyra [Assistant]; Valle, David [Assistant];

ISBN 10: 0801857422 / ISBN 13: 9780801857423

Published by Johns Hopkins University Press, 1998

About this Item

3 volumes--complete. Quarto, 11 1/4" tall, vol. 1: ccclxv + 526 pages; vol. 2: xii + pages 1 to 1930; vol. 3: xii: autosomal, chomosome and mitochondrial catalog pages 1933 to 3612, illustrated boards. A fine, clean, neat hard cover first edition with little shelf wear, gently read, binding tight, paper bright. Without dust jacket, as issued. These are larger and heavier volumes and will require additional postage.

Seller Inventory # 60351

Bibliographic Details

• Title: Mendelian Inheritance in Man: A Catalog of Human Genes and Genetic Disorders [3 volumes, complete] twelfth edition
• Publisher: Johns Hopkins University Press
• Publication Date: 1998
• Language: English
• ISBN 10: 0801857422
• ISBN 13: 9780801857423
• Binding: Hardcover
• Edition: 12th (twelfth) edition.
• Condition: Fine
• Dust Jacket Condition: Without dust jacket
• Weight: 302 ounces
• Seller catalogs:
  • Science

About this title

Synopsis

"The book is a magnificent security blanket for the clinical geneticist and should be in the libraries not only of these specialists, but also of all others who see patients with diseases that have genetic components." ― New England Journal of Medicine

Mendelian Inheritance in Man (MIM) is a genetic knowledgebase that serves clinical medicine and biomedical research, including the Human Genome Project. It aims to be comprehensive (not only complete, but also collated, integrated, and interpreted), authoritative (not only accurate but also sound in its interpretations and judgements), and timely (not only up-to-date but also historically dimensioned).

The twelfth edition of this classic reference work includes:

• More than 2,000 new entries

• A total of more than 9,000 entries

• New features and enhancement of the familiar old features

• Mapping information on more than 4,000 genes of known function

• Information on specific point mutations responsible for more than 700 genetic disorders or neoplasms

About the Author

Victor A. McKusick, M.D., is University Professor of Medical Genetics at the Johns Hopkins University School of Medicine. He was formerly William Osler Professor and Chairman of the Department of Medicine at that institution and Physician-in-Chief of the Johns Hopkins Hospital. He is co-founder and co-director of the Short Course in Medical and Experimental Mammalian Genetics, held annually in Bar Harbor, Maine, since 1960.