Since the first edition of this book appeared in 1983 considerable changes have taken place in many aspects of medical genetics. These have been very largely due to the application of recombinant DNA techniques. This technology has helped our understanding of the fine structure of genes and is also beginning to unravel the molecular pathology of many inherited disorders. But perhaps of more immediate and practical importance, the technology has introduced novel and precise methods for detecting female carriers of X-linked disorders, presymptomatic cases of dominant disorders of late onset and in the prenatal diagnosis of genetic disease. These changes are reflected in most of the contributions to this new edition and their relevance will be apparent in almost all aspects of the subject. In two volumes, this book covers both common and rare genetic disorders. The editors aimed to include all genetic disorders and by drawing contributors from around the world, they obtained a specialist or - in the case of many of the rare disorders - the specialist in that disorder. This edition has been revised but retains the structure of the first edition - scientific principles, reviewed chromosome disorders, system-by-system review of genetic disorders, and applied genetics.
Die Inhaltsangabe kann sich auf eine andere Ausgabe dieses Titels beziehen.
Since the first edition of this book appeared in 1983 considerable changes have taken place in many aspects of medical genetics. These have been very largely due to the application of recombinant DNA techniques. This technology has helped our understanding of the fine structure of genes and is also beginning to unravel the molecular pathology of many inherited disorders. But perhaps of more immediate and practical importance, the technology has introduced novel and precise methods for detecting female carriers of X-linked disorders, presymptomatic cases of dominant disorders of late onset and in the prenatal diagnosis of genetic disease. These changes are reflected in most of the contributions to this new edition and their relevance will be apparent in almost all aspects of the subject. In two volumes, this book covers both common and rare genetic disorders. The editors aimed to include all genetic disorders and by drawing contributors from around the world, they obtained a specialist or - in the case of many of the rare disorders - the specialist in that disorder. This edition has been revised but retains the structure of the first edition - scientific principles, reviewed chromosome disorders, system-by-system review of genetic disorders, and applied genetics.
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Zustand: Good. Volume 1. This is an ex-library book and may have the usual library/used-book markings inside.This book has hardback covers. Clean from markings. In good all round condition. Please note the Image in this listing is a stock photo and may not match the covers of the actual item,2100grams, ISBN:0443035830. Bestandsnummer des Verkäufers 9567857
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Anbieter: BookHolders, Towson, MD, USA
Zustand: Good. [ No Hassle 30 Day Returns ][ Ships Daily ] [ Underlining/Highlighting: NONE ] [ Writing: NONE ] [ Edition: second ] Publisher: Churchill Livingstone Pub Date: 5/1/1990 Binding: Hardcover Pages: 2192 second edition. Bestandsnummer des Verkäufers 5983360
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Anbieter: BookHolders, Towson, MD, USA
Zustand: Good. [ No Hassle 30 Day Returns ][ Ships Daily ] [ Underlining/Highlighting: NONE ] [ Writing: NONE ] [ Edition: second ] Publisher: Churchill Livingstone Pub Date: 5/1/1990 Binding: Hardcover Pages: 2192 second edition. Bestandsnummer des Verkäufers 5983355
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Anbieter: Better World Books, Mishawaka, IN, USA
Zustand: Good. Former library book; may include library markings. Used book that is in clean, average condition without any missing pages. Bestandsnummer des Verkäufers GRP64938667
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