Lynn B. Jorde

Medical Genetics Medical Genetics - illustrated - London Elsevier Masson 2003 - 363 pages

This is one of the few medical genetics texts on a 2-year revision cycle. It provides up-to-date information that can be read, retained, and applied with ease! The 3rd Edition covers pharmacogenomics, the societal implications of technologies, the Human Genome Project, cloning, genetic enhancement, and embryonic stem cell research, new tumor suppressor genes and oncogenes, and more. Mini-summaries, study questions, suggested readings, and a detailed glossary facilitate review of the material. Clinical relevance is demonstrated in over 230 photographs, illustrations, and tables as well as boxes containing patient/family vignettes. Its coverage includes ethical, legal, and social issues and clinical commentary on important genetic diseases. A companion web site offers continuing updates and a wealth of additional features.
Features mini-summaries that appear in bold throughout each chapter.
Supplies study questions and suggested readings at the end of each chapter.
Contains a detailed glossary at the end of the book.
Offers Clinical Commentary boxes that present detailed coverage of the most important genetic diseases and provide examples of modern clinical management.
Demonstrates clinical relevance with boxed patient/family vignettes and coverage of ethical, legal, and social issues.
Provides visual reinforcement and easy access to key information with over 230 photographs, illustrations, and tables.
Includes a companion website with continuing content updates, additional clinical images, and more!
Explores new technologies, including microarrays (e.g., DNA chips) and PCR-free detection of polymorphisms.
Offers new material on pharmacogenomics, a field of study based on the principles of pharmacogenetics where genetic variation is assessed in order to predict a patient's response to specific drugs, including potential adverse reactions.
Includes a new chapter, Genetics and Society, that discusses privacy, discrimination, and the societal implications of new genetic technologies
Devotes a new section to the advances made possible by The Human Genome Project, such as the use of genomics databases to identify disease-causing genes.
Contains a new section on Human Cloning, Genetic Enhancement, and Embryonic Stem Cell Research.
Updates the Cancer Genetics chapter with information on new tumor suppressor genes and oncogenes, including discussion of their roles in carcinogenesis
Expands the section, The Genetics of Common Diseases, with new information on genes predisposing to hypertension, type 2 diabetes, Alzheimer's disease, obesity, heart disease, and stroke.

2842995759 9782842995751 = 2004 Elsevier SAS acides affectés allèles anomalies approximativement association atteints augmentation autosomique bases c'est-à-dire cancer caractère caractéristiques cellulaire cellules chaîne Chapitre chromosome classe clinique codant composé conséquent cours d'ADN d'autres déficit délétion dépistage descendance détection déterminer développement diagnostic différentes dominante effectuée également élevé enfants entraîne environ études exemple existe facteurs familiale famille femmes fonction formation forme fréquemment généralement gènes génétique génique génome groupe Hérédité hétérozygotes humain importante indiqué individus l'ADN l'homme l'un liaison liés loci locus lymphocytes maladie maladies génétiques malformations manière marqueur membres ment mère mesure molécules montré mutations nombre nombreux normal observée parents pathologique patients permet peuvent phénylalanine plupart polymorphismes population portant premier présentant présentent probabilité processus produit protéine provoquée qu'un récepteurs récessive région relativement réservés responsables risque séquence séquence d'ADN sera seulement situés souffrant souvent spécifiques syndrome système Tableau taille taux techniques terme test tion traitement transcription transmission trisomie 21 tumeurs type unique utilisée

-- Medical / Genetics-- Medical › Genetics

616/.042 TUR