Emery Elementos De Genetica Medica By Peter Turnpenny.pdfl
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Emery Elementos De Genetica Medica By Peter Turnpenny.pdfl
Emery Elementos De Genetica Medica: A Comprehensive Textbook on Medical Genetics and Genomics
Emery Elementos De Genetica Medica is a Spanish translation of Emery's Elements of Medical Genetics and Genomics, a leading textbook in this fast-moving field. The book offers current, complete information with a strong basis in practical clinical genetics and genomics for medical school and beyond. The 16th edition of this award-winning text has been thoroughly updated throughout and includes case-based and multiple-choice questions, end-of-chapter summaries, an extensive glossary, and convenient online access.
The book covers the basic principles of human genetics, molecular genetics, genetic disease, chromosomal disorders, single gene disorders, multifactorial inheritance, cancer genetics, pharmacogenetics, epigenetics, developmental genetics, genetic testing and screening, ethical and social issues in genetics, and more. The book also features clinical cases that illustrate the application of genetics to diagnosis and management of various genetic conditions.
Emery Elementos De Genetica Medica is written by Peter D Turnpenny, Sian Ellard, Ruth Cleaver, and translated by Pedro L Donado Pintado, Isabel Campos Adrados, Jose Luis Gonzalez Hernandez. The book is published by Elsevier and available in paperback and ebook formats. The book is suitable for all medical undergraduates as well as postgraduates seeking to improve their understanding and knowledge of medical genetics and genomics.
If you are interested in learning more about Emery Elementos De Genetica Medica, you can visit the publisher's website or find a copy in the library. You can also read some reviews from other readers who have used this book as a reference or a study guide.
Medical genetics and genomics are two related but distinct fields of study that aim to understand the genetic basis of human health and disease. Medical genetics focuses on the diagnosis and management of inherited disorders, such as cystic fibrosis, Huntington's disease, and phenylketonuria. Medical genetics also involves genetic counseling, which helps individuals and families make informed decisions about their genetic risks and options. Medical genetics uses various methods to analyze genes and chromosomes, such as karyotyping, microarray, and sequencing.
Genomics, on the other hand, studies the entire genome of a person or a population, and how it interacts with environmental factors and behaviors. Genomics can reveal the genetic variations that contribute to complex diseases, such as heart disease, asthma, diabetes, and cancer. Genomics can also help identify new targets for therapies and treatments, as well as new diagnostic tools and personalized medicine approaches. Genomics uses advanced technologies, such as next-generation sequencing, bioinformatics, and functional genomics.
Both medical genetics and genomics are important for improving human health and preventing disease. By understanding the genetic and genomic factors that influence health and disease, researchers can develop better strategies for prevention, diagnosis, treatment, and prognosis. Medical genetics and genomics also have ethical, legal, and social implications that need to be addressed by health professionals and policy makers. aa16f39245