Mutations in Human Genetic Disease
by David N. Cooper, Jian-Min Chen
Publisher: InTech 2012
Number of pages: 294
In this volume, a number of different authors from diverse backgrounds describe how the nature, location and frequency of different types of mutation causing inherited disease are shaped in large part, and often in remarkably predictable ways, by the local DNA sequence environment.
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by Nicholas H. Bergman - Humana Press Inc.
A collection of robust protocols for molecular biologists beginning to use comparative genomic analysis tools in a variety of areas. The available chapters describe National Center for Biotechnology Information resources available to the public.
by Digamber S Borgaonkar - National Center for Biotechnology Information
This volume provides an unparalleled means of reviewing the world literature on all common and rare chromosomal alterations and abnormalities. Subject areas: variations and anomalies, numerical anomalies, and chromosomal breakage syndromes.
by Chunsheng Kang - InTech
The aim of this book is to cover key aspects of existing problems in the field of development and future perspectives in gene therapy. Contributions consist of basic and translational research, as well as clinical experiences.
by Marcus Pembrey - Progress Educational Trust
This booklet is a basic introduction to the role of genetics and epigenetics in diseases. It begins by examining conditions where there is a single faulty gene to blame, and moves on to diseases where there are likely to be many contributing factors.