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Diagnostic Techniques in Genetics
Jean-Louis Serre (Edited by), J–L Serre (Author), Isabelle Heath (Translated by), Simon Heath (Translated by)
9780470870259, Wiley
Paperback / softback, published 25 August 2006
270 pages
24.6 x 17 x 1.8 cm, 0.517 kg
"This is a good, solid, basic review of molecular technology. It is a useful companion book of the beginning scholar in human genetics." (Doody's, November 2007)
Einen breit gefacherten Uberblick uber die Anwendungen von DNA- und RNA-Technologien im Rahmen genetischer Diagnosen biette Ihnen dieser Band. Bewusst vermeidet es der Autor, allzu sehr ins Detail zu gehen; er wendet sich an Studenten unterer Semester, legt deshalb besonderen Wert auf Verstandlichkeit und behandelt vorrangig Themen von allgemeinem Interesse, sodass Sie ein solides Fundament fur weiter gehende Spezialisierungen aufbauen konnen.
Preface 1. Techniques and Tools in Molecular Biology Used in Genetic Diagnoses 2. The Diagnosis of Inherited Diseases 3. Molecular Diagnosis in Oncology 4. Applications of Molecular Biology to Cytogenetics 5. Screening and Identification of Pathogenic and Exogenic Agents. 6. Identification Using Genetic Fingerprints 7. Molecular Genetics and Populations Index
List of Contributors
1.1 Nucleic acids
1.2 The different types of genetic material studied
1.3 The enzymatic tools for in vitro treatment of DNA
1.4 DNA fragmentation and study of the fragments
1.5 Selective amplification of a nucleotide sequence
1.6 DNA fragment ligation: recombinant DNA and cloning
1.7 DNA fragment sequencing
1.8 Modification of the sequence of a DNA fragment: site-directed mutagenesis.
1.9 Molecular hybridization techniques and application
1.10 Other techniques to study allelic diversity
2.1 Introduction
2.2 Example diagnoses for autosomal diseases
2.3 Example diagnoses for X-linked diseases
2.4 Neurodegenerative diseases
2.5 References and Bibliography.
3.1 General introduction
3.2 Cellular pathways targeted by the tumour process
3.3 Types of genetic alteration leading to cancer
3.4 Alteration origins: the role of the repair genes
3.5 Benefits of molecular studies to patient healthcare
3.6 Genetic predisposition to cancers
3.7 Genetic tests for cancer predisposition
3.8 Conclusions and perspectives
3.9 References
4.1 Introduction
4.2 Molecular diagnosis of anomalies in the number of chromosomes
4.3 Chromosomal microdeletions
4.4 Uniparental disomies
4.5 Conclusions and perspectives
4.6 References
5.1 Clinical virology
5.2 Clinical bacteriology
5.3 Detection of GMOs
5.4 References and Bibliography
6.1 Introduction
6.2 Genetic fingerprints by the analysis of nuclear DNA
6.2.4 A special case: the Y chromosome sequence
6.3 Genetic fingerprints with mitochondrial DNA
6.4 Society facing the question of genetic fingerprint files.
6.5 Conclusion
6.6 Bibliography
7.1 Hardy–Weinberg equilibrium and measures of genetic diversity
7.4 Diagnosis with genetic testing: cystic fibrosis – an academic case
7.5 Gametic disequilibrium
7.6 Reference and Bibliography
Subject Areas: Biology, life sciences [PS]
