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A guide to cancer genetics in clinical practice

By:

Clark, Sue (ed)

Publication details: Harley : TFM, 2009Description: 1 v. ; 27 cm. (pbk) ; 238 ppISBN:

1903378540
9781903378540 (pbk.) :

Subject(s):

Contents:

Genetics is not complicated; Genetics and cancer; Ethical and legal aspects of cancer genetics; Familial adenomatous polyposis; MYH-associated polyposis; Lynch syndrome (hereditary non-polyposis colorectal cancer); Breast cancer; The gynaecologist and inherited cancer; Multiple endocrine neoplasia syndromes; Neurofibromatosis; Familial gastric cancer; Familial pancreatic cancer; Hamartomatous polyposis syndromes; The future structure of care - cancer genetics

Summary: This book covers the basic concepts of cancer genetics. The common inherited cancer syndromes are each dealt with in greater depth, with the current management outlined. It is aimed at all clinicians who may encounter these conditions in their practice. The book sets out to facilitate identification of high-risk individuals and families, to inform interaction with geneticists and other sub-specialists, to provide a basis for patient management and to simulate interest in these fascinating conditions

Holdings
Item type	Home library	Class number	Status	Date due	Barcode
Book	David Adams Library (Royal Marsden)	QZ 520 CLA (Browse shelf(Opens below))	Available		002092
Book	David Adams Library (Royal Marsden) Shelves	QZ50 CLA (Browse shelf(Opens below))	Available		0000005740

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Previous	QZ 400 GAB The biology of cancer	QZ 400 PEC Molecular biology of cancer : mechanisms, targets and therapeutics	QZ 400 PEL The molecular biology of cancer	QZ 520 CLA A guide to cancer genetics in clinical practice	QZ 570 SHA Cancer - the power of food - food, facts and recipes	QZ 700 JOH Oncological emergencies	QZ 700 JOH Oncological emergencies	Next

This book covers the basic concepts of cancer genetics. The common inherited cancer syndromes are each dealt with in greater depth, with the current management outlined. It is aimed at all clinicians who may encounter these conditions in their practice. The book sets out to facilitate identification of high-risk individuals and families, to inform interaction with geneticists and other sub-specialists, to provide a basis for patient management and to simulate interest in these fascinating conditions

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