DNA Array Image Analysis: Nuts & Bolts
Posted by admin | Posted in Genetics | Posted on 25-10-2010
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DNA Array Image Analysis: Nuts & Bolts
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Histology Image Review CD-ROM Medical Book Details: Paperback: 650 pages Publisher: McGraw-Hill/Appleton & Lange; 1 edition (January 1, 1999) Language: English ISBN-10: 0838537480 ISBN-13: 978-0838537480 //...
Adult Congenital Heart Disease: A Practical Guide Medical Book Details: Paperback: 288 pages Publisher: BMJ Books; 1 edition (June 24, 2005) Language: English ISBN-10: 0727916688 ISBN-13: 978-0727916686 // Medical Book Description: This...
Neurophysiology in Neurosurgery: A Modern Intraoperative... Medical Book Details: By Vedran Deletis, Jay Shils, Publisher: Academic Press Number Of Pages: 512 Publication Date: 2002-08-12 ISBN / ASIN: 0122090365 EAN: 9780122090363 // Medical Book...
Essentials of Pediatric Endoscopic Surgery Medical Book Details: Publisher: Springer Number Of Pages: 572 Publication Date: 2008-11 ISBN-10 / ASIN: 3540783865 ISBN-13 / EAN: 9783540783862 Binding: Hardcover // Medical Book...
Acoustic Neuroma, An Issue of Neurosurgery Clinics... Medical Book Details: Publisher: Saunders Number Of Pages: 240 Publication Date: 2008-06-27 ISBN-10 / ASIN: 1416050949 ISBN-13 / EAN: 9781416050940 Binding: Hardcover // Medical Book Description: Topics...
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DNA Array Image Analysis: Nuts & Bolts
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A comprehensive and detailed overview of the current understanding of the molecular pathology of neuromuscular disorders. For each of 20 disorders, the leading international authorities in the field review: Clinical Features, Pathology, Inheritance, Molecular Genetics, Screening, Prenatal Diagnosis, Prevention and Counseling, Possible treatment by Drug or Gene Therapy.
Neuromuscular Disorders: Clinical and Molecular Genetics
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Microsatellites are short stretches of repeated DNA that show exceptional variability in humans and most other species. This has made microsatellites the genetic marker of choice for most applications, including genetic mapping and studies of evolutionary connections between species and populations. This book details the molecular processes which give rise to microsatellite DNA and then describes the wide range of applications.
Microsatellites: Evolution and Applications
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Microsatellites are short stretches of repeated DNA that show exceptional variability in humans and most other species. This has made microsatellites the genetic marker of choice for most applications, including genetic mapping and studies of evolutionary connections between species and populations. This book details the molecular processes which give rise to microsatellite DNA and then describes the wide range of applications.
Microsatellites: Evolution and Applications
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Outlines the laboratory diagnosis of a selected number of diseases which have relatively high incidence and existing screening programs.
The Laboratory Diagnosis of Selected Inborn Errors of Metabolism
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The seven research papers contained in this volume report the latest and most important findings on topics in genetics that are related to medical practice. In particular the contributions focus on genetic aspects of specific kinds of disorders, including epilepsy, muscular dystrophies, and Huntington’s disease. The book as a whole attests to the growing importance of genetic expertise in the day-to-day practice of medicine.
Genetics of Neurological Disorders
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This multimedia, interactive CD-ROM courseware is designed to address the needs of physicians who wish to incorporate the benefits of our new genomic knowledge into their practices. This resource will enhance understanding of the benefits and limitations of these new genetic technologies and their relevance for patients, families and society. The courseware includes case studies and exercises illustrating the status and progress of genetic and genomic medicine for 17 genetic conditions, as well as information on standards of practice, referrals for genetic counseling, and ethical issues.
CME credits are available through Stanford University School of Medicine.
The New Genetics : Courseware for Physicians. Molecular Concepts, Applications, and Ramifications.
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Type 1 diabetes (T1D) is caused by the auto-immune destruction of pancreatic cells and is characterised by absolute insulin insufficiency. The disease was thought to be the prevalent type of diabetes in children and adolescents, affecting up to 0.1 per cent of the world population. T1D is a typical complex and heterogeneous pathology, occurred in genetically predisposing subjects as a result of harmful influence of non-genetic (environmental) factors. This book explores important research in this field.
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Written by investigators who have devoted many years to the study of autoimmune hepatitis, this book brings together the recent data on the molecular aspects of the target antigens of the cellular and humoral autoreactions, the immunogenetics and other factors relating to susceptibility to the disease, the mechanisms of liver damage, and treatment.
Molecular Basis of Autoimmune Hepatitis
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“Human Genetics, Seventh Edition”, is a non-science majors human genetics text that clearly explains what genes are, how they function, how they interact with the environment, and how our understanding of genetics has changed since completion of the human genome project. It is a clear, modern, and exciting book for citizens who will be responsible for evaluating new medical options, new foods, and new technologies in the age of genomics.
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