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 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 Laura Dean, Johanna McEntyre - NCBI
Guide to the variations in our DNA that influences our risk of developing diabetes. The book introduces the reader to what diabetes is and how it develops. Written for anyone interested in science, patients with diabetes, physicians, students, etc.
- Genetics Home Reference
The handbook presents basic information about genetics in clear language: cells and DNA, how genes work, mutations and health, inheriting genetic conditions, genetic consultation, genetic testing, gene therapy, human genome project, genomic research.
by F. Uchiumi, M. Seki, Y. Furuichi - Frontiers Media SA
In this research topic we will focus on the expression and functions of helicases and their encoding genes, reviewing recent research progresses that provide new insights into development of clinical and pharmaceutical treatments targeting helicases.