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Human genetic disease analysis (cop. 1993)

Public ISBD Titre : Human genetic disease analysis : a practical approach Type de document : texte imprimé Auteurs : Kay E. Davies (19..), Éditeur scientifique Mention d'édition : 2nd edition Editeur : Oxford : IRL Press Année de publication : cop. 1993 Collection : Practical approach series, ISSN 0957-025X Oeuvres / Expressions : Human genetic diseases Importance : 1 vol. (xvi-124 p.) Présentation : ill. Format : 25 cm ISBN/ISSN/EAN : 0-19-963308-8 Langues : Anglais (eng) Index. décimale : 616/. Résumé : This book covers all of the commonly used methods for the analysis and diagnosis of human genetic diseases. The chapters describe the analysis of gene mutations as well as the functional organization of genes and chromosomal regions, keeping up-to-date with recent advances in the field. Revisions in this second edition include sections on PCR and FISH. When the first edition of this book was published, prenatal diagnosis based on DNA analysis was performed in two weeks. The advent of PCR has allowed this process to be completed in just a few hours. PCR has had an impact in almost all areas of molecular medicine and thus all the chapters in this new edition have been significantly revised. The development of fluorescence in situ hybridization (FISH) has been important for both genome analysis and diagnosis. This revolutionary new technology is detailed in this volume. The book will be valuable for scientists working in a pure research environment as well as those in service laboratories analyzing different human disease mutations. Human genetic disease analysis : a practical approach [texte imprimé] / Kay E. Davies (19..), Éditeur scientifique  . -  2nd edition . - Oxford : IRL Press, cop. 1993 . - 1 vol. (xvi-124 p.) : ill. ; 25 cm. - (Practical approach series, ISSN 0957-025X) . ISBN : 0-19-963308-8 Oeuvre : Human genetic diseases Langues : Anglais (eng) Index. décimale : 616/. Résumé : This book covers all of the commonly used methods for the analysis and diagnosis of human genetic diseases. The chapters describe the analysis of gene mutations as well as the functional organization of genes and chromosomal regions, keeping up-to-date with recent advances in the field. Revisions in this second edition include sections on PCR and FISH. When the first edition of this book was published, prenatal diagnosis based on DNA analysis was performed in two weeks. The advent of PCR has allowed this process to be completed in just a few hours. PCR has had an impact in almost all areas of molecular medicine and thus all the chapters in this new edition have been significantly revised. The development of fluorescence in situ hybridization (FISH) has been important for both genome analysis and diagnosis. This revolutionary new technology is detailed in this volume. The book will be valuable for scientists working in a pure research environment as well as those in service laboratories analyzing different human disease mutations.

Exemplaires (1)

Code-barres	Cote	Support	Localisation	Section	Disponibilité
02811	20g-02-06	livres	Bibliothèque de la faculté S.N.V * HARCHE MERIEM*	livres	Consultation sur place Exclu du prêt

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