Hereditary Tumors: From Genes to Clinical Consequences

Hereditary Tumors: From Genes to Clinical Consequences book cover

Hereditary Tumors: From Genes to Clinical Consequences

Author(s): Heike Allgayer (Editor), Helga Rehder (Editor), Simone Fulda (Editor)

  • Publisher: Wiley VCH
  • Publication Date: 17 Dec. 2008
  • Edition: 1st
  • Language: English
  • Print length: 559 pages
  • ISBN-10: 3527320288
  • ISBN-13: 9783527320288

Book Description

Summarizing molecular aspects, diagnostic as well as therapeutic issues, this book is the very first and most comprehensive on hereditary aspects of tumor diseases. All the contributors have been made fellows of the Ingrid zu Solms Foundation due to their outstanding achievements in scientific research, and they discuss here the latest aspects in the diagnosis, disease management, and treatment of hereditary tumor diseases and syndromes. A must-have ready reference for medical and biology students, MDs, PhDs, physicians, and researchers.

Editorial Reviews

Review

“The discussions on genetic counselling and psychological issues are interesting and relevant. The discussion of the basic genetics of inherited cancer provides a useful introduction for someone new to the field.” ( Human Genetics , June 2009)

From the Back Cover

Summarizing molecular aspects, diagnostic as well as therapeutic issues, this book is the very first and most comprehensive on hereditary aspects of tumor diseases. The editors and many contributors have been made fellows of the Ingrid zu Solms Foundation due to their outstanding achievements in scientific research, and they discuss here the latest aspects in the diagnosis, disease management, and treatment of hereditary tumor diseases and syndromes.

From the contents:

  • Hereditary Tumors General Aspects
  • Syndromal Types of Hereditary Tumors
  • Site-Specific Aspects of Hereditary Tumors
  • Genetic Counseling for Hereditary Tumors

    A must-have ready reference for medical and biology students, MDs, PhDs, physicians, and researchers.

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