Human Biochemical Genetics

Specificaties
Paperback, 320 blz. | Engels
Cambridge University Press | 1966
ISBN13: 9780521093927
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Cambridge University Press e druk, 1966 9780521093927
€ 47,11
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Samenvatting

This survey of human inherited metabolic abnormalities, originally published in 1959, was a worthy successor to A. E. Garrod's classic Inborn Errors of Metabolism. An enormous amount of knowledge on this subject had been accumulated in the intermittent period and Professor Harris presents an account that at the time was both precise and concise, as well as being highly readable. The study of human biochemical genetics in 1959 involved material that came from a number of disciplines, of which medicine, genetics, biochemistry, chemical pathology and anthropology were the chief. This book aimed to help direct the attention of investigators in each of these subjects to the results, and the implications of the results, obtained by those working in others. It also attempted to indicate the bearing and significance of these results on what was one of the most fundamental problems in biology, namely the mode of action of the hereditary units – the genes of classical genetics

Specificaties

ISBN13:9780521093927
Taal:Engels
Bindwijze:Paperback
Aantal pagina's:320

Inhoudsopgave

1. Introduction; 2. Some aspects of Mendelian heredity in man; 3. Aminoacid metabolism: 1; 4. Aminoacid metabolism: 21; 5. Variations in carbohydrate metabolism; 6. The human haemoglobins; 7. The blood-group substances; 8. The plasma proteins; 9. Some miscellaneous inherited disorders of metabolism; 10. The problem of gene action; Index.
€ 47,11
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        Human Biochemical Genetics