Genetic
Color Atlas of Genetics
Eberhard Passarge, «Color Atlas of Genetics»
Thieme Medical Publishers | ISBN: 3131003634 | 2006 | File type: PDF | 496 pages pages | 15.18 mb
The aim of this book is to give an account of the scientific field of genetics based on visual displays of selected concepts and related facts. Additional information is presented in the introduction, with a chronological list of important discoveries and advances in the history of genetics, in an appendix with supplementary data in tables, in an extensive glossary explaining genetic terms, and in references, including websites for further in-depth studies. This book is written for two kinds of readers: for students of biology and medicine, as an introductory overview, and for their mentors, as a teaching aid. Other interested individuals will also be able to gain information about current developments and achievements in this rapidly growing field.
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X-Linked Mental Retardation (Oxford Monographs on Medical Genetics)
Roger E. Stevenson, Charles E. Schwartz, Richard J. Schroer, «X-Linked Mental Retardation»
Oxford University Press | ISBN: 0195129814 | 1999-10-28 | File type: PDF | 440 pages | 22.1 mb
This is a comprehensive and up-to-date survey of mental retardation caused by genes on the Xchromosome. Clinical and laboratory data on 130 syndromes are presented in a concise and consistent manner. Each syndrome is defined and information is provided on somatic features, growth and development, neurological signs, cognitive performance, imaging and other laboratory findings, and when possible, the nature and localization of the responsible gene. Craniofacial and other somatic findings are extensively illustrated. A differential matrix accompanies each syndrome description to assist the reader in identifying other X-linked syndromes with overlapping features. As background, the X chromosome and the emergence of the concept of X-linked mental retardation are discussed. X-chromosome maps show the location and mapping limits of the responsible genes. The authors have extensive experience in the clinical and laboratory delineation of X-linked mental retardation. They have described new syndromes, regionally mapped disease loci on the X chromosome, and in several cases isolated the genes responsible for X-linked syndromes.
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Stroke Genetics (Oxford Medical Publications)
Publisher: Oxford University Press, USA | 2003-05-29 | 358 pages | ISBN: 0198515863 | 3.29 MB |
Stroke is a major cause of death and the major cause of adult neurological disability in most of the world. Despite its importance on a population basis, research into the genetics of stroke has lagged behind that of many other disorders. However, the situation is now changing. An increasing number of single gene disorders causing stroke are being described, and there is growing evidence that polygenic factors are important in the risk of apparently "sporadic" stroke. Stroke Genetics provides an up-to-date review of the area, suitable for clinicians treating stroke patients, and both clinical and non-clinical researchers in the field of cerebrovascular disease. The full range of monogenic stroke disorders causing cerebrovascular disease, including ischaemic stroke, intracerebral haemorrhage, aneurysms and arteriovenous malformations, are covered. For each, clinical features, diagnosis, and genetics are described. Increasing evidence suggest that genetic factors are also important for the much more common multifactorial stroke; this evidence is reviewed along with the results of genetic studies in this area. Optimal and novel strategies for investigating multifactorial stroke, including the use of intermediate phenotypes such as intima-media thickness and MRI detected small vessel disease are reviewed. The book concludes by describing a practical approach to investigating patients with stroke for underlying genetic disorders. Also included is a list of useful websites.
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Eberhard Passarge: Color Atlas of Genetics :: 2007
Eberhard Passarge: Color Atlas of Genetics :: 2007
English | PDF Book | 497 pp | RAR 12 M | ISBN 9783131003638 | Publisher: Thieme ~ 3rd edition.
More than ever, a solid understanding of genetics is a fundamental element of all medical and scientific educational programs, across virtually all disciplines. And the applications--and implications--of genetic research are at the heart of current medical scientific debates. Completely updated and revised, The Color Atlas of Genetics is an invaluable guide for students of medicine and biology, clinicians, and anyone else interested in this rapidly evolving field.
More than ever, a solid understanding of genetics is a fundamental element of all medical and scientific educational programs, across virtually all disciplines. And the applications--and implications--of genetic research are at the heart of current medical scientific debates. Completely updated and revised, The Color Atlas of Genetics is an invaluable guide for students of medicine and biology, clinicians, and anyone else interested in this rapidly evolving field.
The latest 3rd edition of this highly praised atlas retains several popular features, such as the accessible layout and logical structure, in addition to many novel features and 20 completely new color plates on new topics, including:
* Cell-to-cell communication, including important signaling and metabolic pathways
* Taxonomy of living organisms ("tree of life")
* Epigenetic modifications in chromatin
* Apoptosis
* RNA interference (RNAi)
* Comparative genomic hybridization
* Origins of cancer
* Principles of gene and stem cell therapy, etc.
With more than 200 absorbing full-color plates concisely explained on facing page, the atlas offers readers an easy-to-use, yet remarkably detailed guide to key molecular, theoretical, and medical aspects of genetics and genomics. Brief descriptions of numerous genetic diseases are included, with references for more detailed information.
Readers will find that this incomparable book presents a comprehensive picture of the field from its fascinating history to its most advanced applications.
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ABC of Clinical Genetics
Helen M. Kingston , ?ABC of Clinical Genetics?
BMJ Publishing Group | ISBN 0727916270 | February 2002 | PDF | 120 Pages | 1641 Kb
Medical Journal of Australia, Spring 2003
There is now no excuse for anyone to claim that he (she) does not understand clinical genetics.
Book Description:
This ABC is a concise, highly illustrated introduction to genetic mechanisms involved in inherited disorders. The new edition has been extensively updated with new and revised chapters to encompass rapid advances in the field. Basic genetic concepts are explained along with the application of new technologies in clinical practice. Information on relevant web sitesare also included along with recommended texts for further reading.
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All About Albumin: Biochemistry, Genetics, and Medical Applications
All About Albumin: Biochemistry, Genetics, and Medical Applications
Publisher: Academic Press | ISBN: 0125521103 | edition 1995 | File type: PDF | 432 pages | 24 mb
Ted Peters brings these diverse aspects of the proteins fascination together with a relaxed stylein this definitive volume on albumin and its homologues. The huge ensuing literature has been expertly distilled into an understandable account of its binding properties, which are interpreted in the context of the three-dimensional structure, recently determined by Carter and colleagues. The heart shape and heart of the molecule is exposed in a number of elegant colour plates, andresidues involved in binding are clearly displayed in a reconfiguration of the familiar disulphide-bonded model. The student of molecular genetics and protein evolution will find a clear interpretation of the relationships. There is also an up-to-the minute account of human albumin mutations.
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